W81K0219Q0083_SOLICITATION.pdf

PDF 703 KB Posted Mar 27, 2019

Attached to: Reagents with Chemistry and Immunology Analyzers
Solicitation number: W81K0219Q0083
Issued by: Department of the Army Medical Command

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SEE ADDENDUM

(No Collect Calls)

W81K0219Q0083 27-Mar-2019

b. TELEPHONE NUMBER

808-438-5105

8. OFFER DUE DATE/LOCAL TIME

10:00 AM 12 Apr 2019

5. SOLICITATION NUMBER 6. SOLICITATION ISSUE DATE

AUTHORIZED FOR LOCAL REPRODUCTION

PREVIOUS EDITION IS NOT USABLE

STANDARD FORM 1449 (REV. 2/2012)

Prescribed by GSA – FAR (48 CFR) 53.212

(TYPE OR PRINT)

(SIGNATURE OF CONTRACTING OFFICER)

ADDENDA ARE

26. TOTAL AWARD AMOUNT (For Gov t. Use Only )

23.

CODE 10. THIS ACQUISITION IS

SUCH ADDRESS IN OFFER

17b. CHECK IF REMITTANCE IS DIFFERENT AND PUT

BELOW IS CHECKED

TELEPHONE NO.

W81K029. ISSUED BY

18b. SUBMIT INVOICES TO ADDRESS SHOWN IN BLOCK 18a. UNLESS BLOCK

7. FOR SOLICITATION

INFORMATION CALL:

a. NAME

TAE H. KIM

2. CONTRACT NO. 3. AWARD/EFFECTIVE DATE 4. ORDER NUMBER

(TYPE OR PRINT)

30b. NAME AND TITLE OF SIGNER 30c. DATE SIGNED 31b. NAME OF CONTRACTING OFFICER

30a. SIGNATURE OF OFFEROR/CONTRACTOR 31a.UNITED STATES OF AMERICA

0 27a. SOLICITATION INCORPORATES BY REFERENCE FAR 52.212-1. 52.212-4. FAR 52.212-3. 52.212-5 ARE ATTACHED.

25. ACCOUNTING AND APPROPRIATION DATA

1. REQUISITION NUMBER

20.

ADDITIONAL SHEETS SUBJECT TO THE TERMS AND CONDITIONS SPECIFIED.

OFFEROR TO COMPLETE BLOCKS 12, 17, 23, 24, AND 30

SOLICITATION/CONTRACT/ORDER FOR COMMERCIAL ITEMS

0011298905

ARE NOT ATTACHED

27b. CONTRACT/PURCHASE ORDER INCORPORATES BY REFERENCE FAR 52.212-4. FAR 52.212-5 IS ATTACHED. ADDENDA ARE ARE NOT ATTACHED

(BLOCK 5), INCLUDING ANY ADDITIONS OR CHANGES WHICH ARE

SET FORTH HEREIN, IS ACCEPTED AS TO ITEMS:

. YOUR OFFER ON SOLICITATION

28. CONTRACTOR IS REQUIRED TO SIGN THIS DOCUMENT AND RETURN

% FOR:SET ASIDE:UNRESTRICTED ORX

SMALL BUSINESS

17a.CONTRACTOR/ CODE FACILITY

OFFEROR CODE

W40M REGIONAL HEALTH CONTRACTING OF

REGIONAL HEALTH CONTR OFC PACIFIC

BLDG 339 CLARK ROAD

FT SHAFTER HI 96858-5098

18a. PAYMENT WILL BE MADE BY CODE

RATED ORDER UNDER

DPAS (15 CFR 700)

13a. THIS CONTRACT IS A

13b. RATING

CODE15. DELIVER TO CODE W80MAX 16. ADMINISTERED BY

12. DISCOUNT TERMS11. DELIVERY FOR FOB DESTINA-

TION UNLESS BLOCK IS

MARKED

SEE SCHEDULE

14. METHOD OF SOLICITATION

RFQ IFB RFPX

W6R0 USA MED DEPT ACT KOREA

DIR DEL SEE LINE ITEM(S)

USA MED MATERIAL CTR KOREA

BLDG 709 CAMP CARROLL

WAEGWAN 718 800

TEL: , FAX: ,

.FAX:

TEL: . SERVICE-DISABLED

VETERAN-OWNED

SMALL BUSINESS

8(A)

HUBZONE SMALL

BUSINESS

SIZE STANDARD:

1,250

NAICS:

325413

OFFER DATED

29. AWARD OF CONTRACT: REF.

DELIVER ALL ITEMS SET FORTH OR OTHERWISE IDENTIFIED ABOVE AND ON ANY

COPIES TO ISSUING OFFICE. CONTRACTOR AGREES TO FURNISH AND

EMAIL:

TEL:

31c. DATE SIGNED

SEE SCHEDULE

SCHEDULE OF SUPPLIES/ SERVICESITEM NO. QUANTITY UNIT UNIT PRICE AMOUNT

24.22.21.19.

WOMEN-OWNED SMALL BUSINESS (WOSB)

ELIGIBLE UNDER THE WOMEN-OWNED

SMALL BUSINESS PROGRAM

EDWOSB

32g. E-MAIL OF AUTHORIZED GOVERNMENT REPRESENTATIVE

SOLICITATION/CONTRACT/ORDER FOR COMMERCIAL ITEMS

(CONTINUED)

PAGE 2 OF86

ACCEPTED, AND CONFORMS TO THE CONTRACT, EXCEPT AS NOTED: ______________________________________________________

32a. QUANTITY IN COLUMN 21 HAS BEEN

RECEIVED INSPECTED

32b. SIGNATURE OF AUTHORIZED GOVERNMENT

REPRESENTATIVE

32c. DATE 32d. PRINTED NAME AND TITLE OF AUTHORIZED GOVERNMENT

REPRESENTATIVE

32e. MAILING ADDRESS OF AUTHORIZED GOVERNMENT REPRESENTATIVE 32f . TELEPHONE NUMBER OF AUTHORIZED GOVERNMENT REPRESENTATIVE

37. CHECK NUMBER

FINALPARTIALCOMPLETE

36. PAYMENT35. AMOUNT VERIFIED

CORRECT FOR

34. VOUCHER NUMBER

FINAL

33. SHIP NUMBER

PARTIAL

38. S/R ACCOUNT NUMBER 39. S/R VOUCHER NUMBER 40. PAID BY

41a. I CERTIFY THIS ACCOUNT IS CORRECT AND PROPER FOR PAYMENT

41b. SIGNATURE AND TITLE OF CERTIFYING OFFICER 41c. DATE

42a. RECEIVED BY (Print)

42b. RECEIVED AT (Location)

42c. DATE REC'D (YY/MM/DD) 42d. TOTAL CONTAINERS

STANDARD FORM 1449 (REV. 2/2012) BACK

Prescribed by GSA – FAR (48 CFR) 53.212

AUTHORIZED FOR LOCAL REPRODUCTION

PREVIOUS EDITION IS NOT USABLE

SEE SCHEDULE

20.

SCHEDULE OF SUPPLIES/ SERVICES

21.

QUANTITY UNIT

22. 23.

UNIT PRICE

24.

AMOUNT

19.

ITEM NO.

W81K0219Q0083

Section SF 1449 - CONTINUATION SHEET

ITEM NO SUPPLIES/SERVICES MAX

QUANTITY

UNIT UNIT PRICE MAX AMOUNT

0001 2 Job

TEST REAGENTS

FFP

BASE PERIOD: 01 JUNE 2019 - 30 SEPTEMBER 2019

Test Reagents Including Lease VITROS XT7600

BRAND NAME OR EQUAL

Unit of Measure "JOB" will allow for multiple invoice payments to be made against this CLIN. At no point shall the quantities exceed the set quantities listed on Attachment 2.

SEE ATTACHMENT 2 for Quantities

Enter per reagent price in ATTACHMENT 3

PROCUREMENT INCLUDES ALL MAINTENANCE AND TROUBLE

CALLS AS NEEDED.

FOB: Destination

PURCHASE REQUEST NUMBER: 0011298905

MFR PART NR: NA

PSC CD: 6515

MAX

NET AMT

UNIT UNIT PRICE MAX AMOUNT

1001 4 Job

OPTION TEST REAGENTS

FFP

OPTION I PERIOD: 01 OCTOBER 2019 - 30 SEPTEMBER 2020

Test Reagents Including Lease VITROS XT7600

BRAND NAME OR EQUAL

Unit of Measure "JOB" will allow for multiple invoice payments to be made against this CLIN. At no point shall the quantities exceed the set quantities listed on Attachment 2.

SEE ATTACHMENT 2 for Quantities

Enter per reagent price in ATTACHMENT 3

PROCUREMENT INCLUDES ALL MAINTENANCE AND TROUBLE

CALLS AS NEEDED.

FOB: Destination

UNIT UNIT PRICE MAX AMOUNT

1002 1 Job

OPTION RELOCATION

FFP

OPTION I PERIOD: 01 OCTOBER 2019 - 30 SEPTEMBER 2020

Moving One Unit of XT7600 from SGT Jenkins Clinic to 121st CSH BAACH.

Exact date is TBD

Enter relocation cost price in ATTACHMENT 3

FOB: Destination

UNIT UNIT PRICE MAX AMOUNT

2001 4 Job

OPTION TEST REAGENTS

FFP

OPTION II PERIOD: 01 OCTOBER 2020 - 30 SEPTEMBER 2021

Test Reagents Including Lease VITROS XT7600

BRAND NAME OR EQUAL

Unit of Measure "JOB" will allow for multiple invoice payments to be made against this CLIN. At no point shall the quantities exceed the set quantities listed on Attachment 2.

SEE ATTACHMENT 2 for Quantities

Enter per reagent price in ATTACHMENT 3

PROCUREMENT INCLUDES ALL MAINTENANCE AND TROUBLE

CALLS AS NEEDED.

FOB: Destination

UNIT UNIT PRICE MAX AMOUNT

3001 4 Job

OPTION TEST REAGENTS

FFP

OPTION III PERIOD: 01 OCTOBER 2021 - 30 SEPTEMBER 2022

Test Reagents Including Lease VITROS XT7600

BRAND NAME OR EQUAL

Unit of Measure "JOB" will allow for multiple invoice payments to be made against this CLIN. At no point shall the quantities exceed the set quantities listed on Attachment 2.

SEE ATTACHMENT 2 for Quantities

Enter per reagent price in ATTACHMENT 3

PROCUREMENT INCLUDES ALL MAINTENANCE AND TROUBLE

CALLS AS NEEDED.

FOB: Destination

UNIT UNIT PRICE MAX AMOUNT

4001 4 Job

OPTION TEST REAGENTS

FFP

OPTION IV PERIOD: 01 OCTOBER 2022 - 30 SEPTEMBER 2023

Test Reagents Including Lease VITROS XT7600

BRAND NAME OR EQUAL

UUnit of Measure "JOB" will allow for multiple invoice payments to be made against this CLIN. At no point shall the quantities exceed the set quantities listed on Attachment 2.

SEE ATTACHMENT 2 for Quantities

Enter per reagent price in ATTACHMENT 3

PROCUREMENT INCLUDES ALL MAINTENANCE AND TROUBLE

CALLS AS NEEDED.

FOB: Destination

INSPECTION AND ACCEPTANCE TERMS

Supplies/services will be inspected/accepted at:

CLIN INSPECT AT INSPECT BY ACCEPT AT ACCEPT BY

0001 Destination Government Destination Government 1001 Destination Government Destination Government 1002 Destination Government Destination Government 2001 Destination Government Destination Government 3001 Destination Government Destination Government 4001 Destination Government Destination Government

DELIVERY INFORMATION

CLIN DELIVERY DATE QUANTITY SHIP TO ADDRESS DODAAC /

CAGE

0001 POP 01-JUN-2019 TO

30-SEP-2019

N/A W6R0 USA MED DEPT ACT KOREA

DIR DEL SEE LINE ITEM(S)

USA MED MATERIAL CTR KOREA

BLDG 709 CAMP CARROLL

WAEGWAN 718 800

W80MAX

1001 POP 01-OCT-2019 TO

30-SEP-2020

N/A (SAME AS PREVIOUS LOCATION)

1002 POP 01-OCT-2019 TO

30-SEP-2020

N/A (SAME AS PREVIOUS LOCATION)

2001 POP 01-OCT-2020 TO

30-SEP-2021

N/A (SAME AS PREVIOUS LOCATION)

3001 POP 01-OCT-2021 TO

30-SEP-2022

N/A (SAME AS PREVIOUS LOCATION)

4001 POP 01-OCT-2022 TO

30-SEP-2023

N/A (SAME AS PREVIOUS LOCATION)

ATTACHMENT 1 - SALIENT CHARACT

Salient Characteristics

The Contractor shall provide two (2) fully automated, discrete random access chemistry and immunology analyzers capable of providing a complete chemistry and immunochemistry testing. The entire analyzer system shall be serviced and supplied through a single Contractor (to whom the contract is awarded), including any parts, equipment, or supplies not manufactured, provided or serviced by the Contractor. The system shall provide redundancy (to ensure continuous operations.). The Contractor shall provide the system, training, supplies, reagents, unscheduled maintenance, and preventive maintenance for the system. All equipment displays and supporting literature shall be in the English language. The Contractor shall include delivery, installation, all calibrator/standards, reagents/reagent packs, and quality control materials necessary to perform the specified assays, initial Method Validations per the Clinical Laboratory Standards Institute (CLSI) guidelines and the Department of Pathology and Laboratory Services (DPALS) Quality Manual (QM). The Contractor shall also provide analyzer removal at the termination of the contract.

The analyzer system shall include at a minimum:

1) Dry Chemistry Testing

2) Apply Digital Refractometer

3) All peripherals required for the analyzer system to be useable. (e.g. Uninterrupted Power Sources (UPS), instrument specific computer terminals and CPUs, etc.)

4) Fully automated and discrete random access

5) Simple or no reagent preparation, easy reagent loading on the analyzer. No manual primes, washes or tubing maintenance.

6) Shall detect clot, bubble, low and high viscosity, short sample detection and liquid level sensing.

7) Shall detect and flag results due to hemolysis, icterus, and turbidity.

8) Shall perform auto re-run, auto reflex dilution for sample distribution.

9) The system shall have a data management system for storage of patient results, quality control and preventive maintenance data. System shall have a bi-directional interface to the analyzer and to the hospital information system

(CHCS).

10) All models shall perform satisfactorily any laboratory temperature between 68 and 80 degrees Fahrenheit and at any laboratory relative humidity between 40 and 75%.

11) Uninterruptable power source capable of providing all necessary electrical power to the analyzer and data management system.

12) All equipment displays and literature shall be in English.

13) Stat Testing interrupt capability.

14) Initial start up to shut down shall not exceed 20 minutes.

15) Analyzers and supplies shall be FDA approved.

16) Analyzer shall perform environmental monitoring of optimal temperature or humidity of incubators, ambient condition, and reagents supplies. Parameters are 36.0 – 38.0 ºC of incubator temperature, 20.0 – 28.0 ºC of ambient temperature, 14.0 – 24.0 ºC of reagent supplies temperature, and 5.0 - 38.0 ºC of supplies humidity.

17) The total length of the instrument shall not exceed: Width – 9.5 feet; Depth – 3 feet; Height – 6 feet.

18) Minimum 7 days on board calibration stability.

19) System shall be capable of performing the FDA approved tests listed in Minimum/Maximum Ordering

Amounts.

20) The analyzer systems will be located at:

Brian Allgood Army Community Hospital (BAACH) Building 3030/3031 Unit #15190 APO AP 96271-5190 USAG-Humphreys

MSG Henry L. Jenkins Patient Centered Medical Home (PCMH) Building S-555 Unit #15190 APO AP 92671-5190 Camp Humphreys, Korea

* The analyzer located in PCMH will need to be moved to BAACH in November 2019 (exact date of the relocation is TBD)

21) The Contractor is required to provide new state of the art equipment. Discontinued models are not acceptable.

22) Within 10 working days after contract award, the Contractor shall coordinate and conduct a post award site visit for the purpose of coordinating schedule for equipment installation.

Method Validation shall be conducted in accordance with method validation protocols established by the Department of Pathology’s Quality Management Program (those protocols are in accordance with applicable standards as described by the Clinical Laboratory Standards Institute (CLSI) and/or required by the College of American Pathologists (CAP)).

Method Validation shall include but not be limited to, normal range verification, demonstration of linearity, reportable range, correlation with current methods (comparison of methods study), validation of precision (replication study) and accuracy (recovery study), calibration, and establishment of initial control ranges using control materials, to include third party controls, as designated by the Laboratory Director.

Method Validation shall be completed and approved by the Medical Director prior to reporting of patient results.

Payment for services shall not begin until the analyzer system has been approved for reporting of patient results.

The Contractor shall provide a qualified Technical Service Representative, who possesses a thorough knowledge of method validation and is familiar with the use of statistical evaluation software as determined by the Laboratory Manager, to provide technical assistance for the method validation studies. The assigned Technical Service Representative shall be responsible for the entire Method Validation.

All reagents, calibrators and linearity materials used in the Method Validation Study shall be provided be the Contractor at no additional cost to the Government. These materials shall not be used in the analysis of specimens for patient care.

The Government’s Technical Supervisor shall obtain patient specimens for use in the Method Validation. In the event that specimen requirements for correlation studies cannot be met (e.g., insufficient number of patients to challenge the extremes of a curve), the Contractor shall assist in procuring additional specimens. These specimens may be obtained from other laboratories from Contractor sources.

Both the Contractor and Contractor personnel at each location shall abide by all Health Insurance Portability & Accountability Act of 1996 (HIPAA) rules and regulations when conducting the Method Validation Study.

The Contractor shall provide two (2) paper and two (2) CD copies of the Operator’s and Maintenance manuals and a statement of the warranty terms in the English language. The level of detail required of appropriate instrument maintenance manuals extends on to routine maintenance procedures performed by the user. All instrumentation specified is non-Government owned, leased, equipment that is serviced and maintained by the Contractor.

The Contractor shall provide safety data sheets (SDS) for each item delivered under this contract that is considered to be HAZARDOUS MATERIAL by the United States or the government representative. The SDS shall contain information on the hazards associated with each specific chemical or material. The SDS shall be printed in the English language and shall contain, as a minimum, identification of:

1) The hazardous material

2) The specific hazard

3) The required practices for the safe use of the product

4) First aid procedures

5) What to do in the event of a spill or other mishap or accident

The Contractor shall provide the reagents and shall coordinate exact quantities and shipment schedule with the government personnel prior to shipment IAW Deliveries (below).

The Contractor shall be responsible for the collection and transportation of equipment upon termination of the contract.

Reagents

1) Reagent package unit shall be appropriate regarding the workload and on board stability to minimize the loss of reagents. For example, for low volume tests, reagent packages shall be small enough to minimize having to throw out reagents due to non-use and has met expiration date.

2) The reagents for therapeutic drug monitoring such as Salicylate, Acetaminophen, Gentamicin, and Vancomycin (not frequently used in Korea) shall be supplied within 7 days after the order is placed.

3) Reagents shall be provided bearing the same lot number within the designated shipments. These items shall be the highest quality, sensitive, specific and tested to assure precision and accuracy. The Contractor shall provide stock that meets proficiency testing standards of the College of American Pathologist (CAP), The Joint Commission (TJC), the Clinical Laboratory Standards Institute (CLSI) and be approved by the Food and Drug Administration

(FDA).

4) Emergency supply orders except for reagents listed in #2 shall be delivered within 48 hours after the order is placed and be of the same lot number of calibrators, reagents and controls currently in use. Emergency supplies are determined by the Government Representative.

5) Non-emergency supply orders except for reagents listed in #2 shall be delivered within 72 hours after the order is placed and be of the same lot number of calibrators, reagents, and controls currently in use. Non-emergency supplies are determined by the Government Representative.

6) Shelf life of reagents shall be at least 3 months from the delivery date. Controls shall have a minimum shelf life of four (4) weeks upon receipt by the Government. If this shelf life requirement cannot be met, the Contractor shall identify the guaranteed shelf life after that can be accommodated in their response to the Request for Quote.

7) The Contractor shall sequester the required quality control materials and test reagents.

8) All reagents provided shall be identical to those used in the FDA 510K approval application. All reagents/reagent packs shall be provided as follow:

a. Shall be provided by the manufacturer of the equipment.

b. Shall be marked with the required storage temperature.

c. Shall be inclusive of an English language package inserts.

9) If the bulk reagents are produced overseas, they shall be manufactured in conformance with ISO or CE standards AND shall be equal to or better than the U.S. products in quality/manufacturing. Documentation of item equivalency shall be provided.

10) Preservation and packing shall be performed in accordance with the best commercial practice and in such a manner to afford adequate protection against any damage during shipment from source to destination.

11) Shall be maintained at the proper storage temperature during transportation from the Contractor’s storage facility to the Government acceptance site and be delivered on time at the appropriate storage temperature.

The actual workload may fluctuate in the fiscal year of the contract due to changes in the distribution of patient care.

In addition, workload may expand in subsequent option years due to fluctuations in patient volume, and with the inclusion of other locations within the USA MEDDAC-K. Minimum/Maximum Ordering Amounts provide the estimated workload for Base Year as well as an estimated workload for each option year.

The Contractor shall provide quality control materials IAW requirements outlined in the Laboratory QA program and approved by the Laboratory Director/Laboratory Manager. This includes third-party controls where requested/required by the laboratory.

The Contractor shall ensure that requirements for routine quality control runs (as defined by the Laboratory Director/Laboratory Manager and outlined in the Laboratory QA program), routine calibration, and periodic calibration/calibration verification (i.e., each assay must be calibrated or have calibration verification performed at intervals not to exceed a 6-month period of time), and for troubleshooting of out-of-control assays be considered when calculating the yearly requirements.

The Contractor shall estimate the volume of user-replaceable maintenance items that shall be required to support the analyzer, and any analyzer specific tools/supplies necessary to perform operator-level periodic maintenance tasks, at the level of use specified in Minimum/Maximum Ordering Amounts. An operator level maintenance tool/spare parts kit shall be provided and replenishment of all expended items shall be made by the contractor, at no additional cost to the Government. Replenishment shall be made as needed or on a periodic basis not to exceed the normal preventive maintenance cycle.

ATTACHMENT 2 - MIN/MAX ORDERIN

MIN/MAX ORDERING AMOUNTS

MINIMUM/MAXIMUM ORDERING ESTIMATES

The minimum guaranteed amount is $10,000.00 and applies only to the base period of performance, 01 June 2019 – 30 September 2019. The maximum quantities are provided below and applies to the full duration of the contract.

The estimated and maximum quantities are included below. The quoter’s price will be evaluated based on the estimated quantities listed below. The total contract award value will be the price of each reagents multiplied by the maximum quantities listed below.

BASE YEAR: 01 JUNE 2019 – 30 SEPTEMBER 2019

Reagent Unit Estimated Quantity

Maximum Quantity

1. Acetaminophone (ACET) 5 Pack/90 Slides Box 5 8

2. Anti-Hepatitis A Virus Immunoglobulin M (A-HAV IGM) 100 Wells Box 7 12

3. Anti-Hepatitis A Virus Immunoglobulin M Calibrator (A-HAV IGM CAL) 1 Level/1 Set

Box 2 4

4. Anti-Hepatitis A Virus Immunoglobulin M Control (A-HAV IGM CONTROL) 2 Levels/3 Sets

Box 5 8

5. Anti-Hepatitis A Virus (A-HAV) TOT 100 Wells Box 4 6

6. Anti-Hepatitis A Virus (A-HAV) Total Calibrator 1 Level/1 Vial Box 2 4

7. Anti-Hepatitis A Virus (A-HAV) Total Control 2 Levels/3 Sets Box 4 7

8. Anti-Hepatitis B Virus Core Antigen (ECI A-HBC) 100 Wells Box 8 14

9. Anti-Hepatitis B Virus Core Antigen (ECI A-HBC) Calibrator Box/1 Set Box 2 4

10. Anti-Hepatitis B Virus Core Antigen (ECI A-HBC) Control Box/3 Set Box 4 6

11. Anti-Hepatitis B Virus Surface Antigen (A-HBS) 100 Wells Box 7 12

12. Anti-Hepatitis B Virus Surface Antigen (A-HBS) Calibrator Box/1 Set Box 2 4

13. Anti-Hepatitis B Virus Surface Antigen (A-HBS) Control Box/3 Sets Box 5 8

14. Anti-Hepatitis C Virus (A-HCV) 100 Wells Box 8 14

15. Anti-Hepatitis C Virus Calibrator (A-HCV CAL) Box/1 Set Box 2 4

16. Anti-Hepatitis C Virus Control (A-HCV CNTL) Box/3 Set Box 4 6

17. Albumin (ALB) 5 Pack/250 Slides Box 11 18

18. Alcohol 5 Pack/90 Slides Box 6 10

19. Alkaline Phophatase (ALKP) 5 Pack/300 Slides Box 9 16

20. Alanine Aminotransferase (ALTV) 5 Pack/300 Slides Box 9 16

21. Amylase 5 Pack/90 Slides Box 5 8

22. Aspartate Aminotransferase (AST) 5 Pack/300 Slides Box 8 14

23. Bilirubin Unconjugated, Bilirubin Conjugated (BUBC) 5 Pack/90 Slides Box 6 10

24. Blood Urea Nitrogen (BUN) 5 Pack/300 Slides Box 8 14

25. Calcium (CA) 5 Pack/300 Slides Box 8 14

26. Calibrator Kit 1 3 Levels/4 Sets Box 1 2

27. Calibrator Kit 2 4 Levels/4 Sets Box 1 2

28. Calibrator Kit 3 3 Levels/4 Sets Box 1 2

29. Calibrator Kit 4 (ALB, BuBc, Fe, TBIL, TIBC, TOTAL PROTEIN) 4 Levels/4 Sets

Box 1 2

30. Calibrator Kit 5 (AMON, PROT) 3 Levels/4 Sets Box 1 2

31. Calibrator Kit 6 (CHE, CKMB) 3 Levels/4 Sets Box 1 2

32. Calibrator Kit 7 3 Levels/2 Sets Box 2 4

33. Calibrator Kit 8 3 Levels/2 Sets Box 1 2

34. Calibrator Kit 9 (ACET, CRBM, DGXN, PHBR, PHTY) 3 Levels/2 Sets Box 2 4

35. Calibrator Kit 10 3 Levels/2 Sets Box 1 2

36. Calibrator Kit 11 6 Levels/1 Set Box 1 2

37. Calibrator Kit 13 6 Levels/1 Set Box 1 2

38. Calibrator Kit 25 3 Levels/2 Sets Box 1 2

39. Calibrator Kit 31 4 Levels/3 Sets Box 1 2

40. Cerebrospinal Fluid (CSF) Protein 5 Pack/90 Slides Box 5 8

41. Cholesterol (CHOL) 5 Pack/300 Slides Box 8 14

42. Creatinine Kinase MB (CKMB) 5 Pack/90 Slides Box 4 7

43. CLINIQA Liquid QCTM Cardiac Marker Control (CLINIQA LIQ CARDIAC MKR CT VS) 1 Unit

Box 3 5

44. C-Reactive Protein (CRP) 5 Pack/90 Slides Box 12 20

45. C-Reactive Protein Performance (CRP PERF) VERIFIER I 2 Levels/6 Vials

Box 4 7

46. C-Reactive Protein Performance (CRP PERF) VERIFIER II 2 Levels/6 Vials

Box 4 7

47. Creatine Kinase (CK) 5 Pack/90 Slides Box 5 8

48. Creatinine/Isotope Diluation Mass Spectometry Standard (IDMS STD) 5 Pack/300 Slides

Box 9 16

49. DESICCANT PACKS Box/2 Sets Box 7 12

50. Diluent Pack 2 3 Packs Box 1 2

51. Diluent Pack 3 3 Packs Box 2 4

52. Direct High Density Lopoprotection (HDL) 5 Pack/300 Slides Box 11 18

53. Enzymatic CO2 (ECO2) 5 Pack/300 Slides Box 11 18

54. Free Thyroid Control (Free T Control) 3 Levels/3 Sets Box 7 12

55. Free T4 100 Wells Box 13 22

56. Free T4 Calibrator 3 Levels/3 Sets Box 2 4

57. FS Air Filter 1 Filter Box 1 2

58. FS CUVETTES Box/6000 Box 1 2

59. FS Humidifaction Packs 6 Packs Box 1 2

60. FS Micro Tip 4096 Tips Box 1 2

61. Gamma Glutamyl Transferase (GGT) 5 pack/250 Slides Box 5 8

62. Gentamicin Reagent (GENT) Box/300T Box 1 2

63. Glucose (GLU) 5 Pack/300 Slides Box 11 18

64. Hepatitis B Virus Antigen (JBSAG) 100 Wells Box 11 18

65. Hepatitis B Virus Antigen Calibrator (HBSAG CAL) Box/1 Vial Box 2 4

66. Hepatitis B Virus Antigen Control (HBSAG CNTL) Box/3 Sets Box 4 7

67. HI SAM DIL A (ON) 100WLS 1 Pack Box 4 6

68. HI SAM DIL B (ON) 100WLS 1 Pack Box 9 16

69. Immuno-Wash Fluid Box/30 Bottles Box 2 4

70. ISOENZYME Performance VERIFIER I (ISO PERF VERIFIER I) 2 Levels/6 Vials

Box 4 6

71. ISOENZYME Performance VERIFIER I (ISO PERF VERIFIER II) 2 Levels/6 Vials

Box 4 6

72. Lactate (LAC) 5 Pack/90 Slides Box 5 8

73. Lactate Dehydrogenase (Traceable to IFCC Reference Method) (LDHI) 5 Pack/250 Slides

Box 6 10

74. Lipase (LIP) 5 Pack/90 Slides Box 6 10

75. LIQUID Performance VERIFIER I (LIQ PERF VERIFIER I) 2 Levels/6 Vials

Box 5 8

76. LIQUID Performance VERIFIER II (LIQ PERF VERIFIER II) 2 Levels/6 Vials

Box 5 8

77. Magnesium (Mg) 5 Pack/300 Slides Box 4 7

78. Maintenance Pack Box/2 Packs Box 2 4

79. Micro Sample Cup 4000 Cups Box 5 8

80. MICROSNS CK FLS I&II Box/2 Sets Box 1 2

81. Perform Verifier I 2 Levels/12 Vials Box 5 8

82. Perform Verifier II 2 Levels/12 Vials Box 5 8

83. Phosphorus (PHOS) 5 Pack/300 Slides Box 3 5

84. Potassium (K+) 5 Pack/250 Slides Box 12 20

85. Reconstitution Diluent 12 Vials Box 1 2

86. Reflectometer Lamp 3 Box 2 4

87. REP ENDO CNTL 3 Levels/3 Sets Box 8 14

88. Rubella Immunoglobulin G (RUBELLA IGG) 100 Wells Box 4 6

89. Rubella Immunoglobulin G (RUBELLA IGG) Calibrator (CAL) 3 Levels/1 Set

Box 2 4

90. Salicylate 5 Pack/90 Slides Box 4 6

91. Sample Cup Pierceable Cap 1000 Caps Box 1 2

92. Signal Reagent Box/2 Packs Box 30 52

93. Sodium (NA+) 5 Pack/250 Slides Box 14 24

94. Therapeutic Drug Monitoring (TDM) PERF VERIFIER I 3 Levels/6 Vials Box 2 4

95. Therapeutic Drug Monitoring (TDM) PERF VERIFIER II 3 Levels/6 Vials Box 2 4

96. Therapeutic Drug Monitoring (TDM) PERF VERIFIER III 3 Levels/6 Vials

Box 2 4

97. TORCH Negative Control Box 1 2

98. TORCH Positive Control Box 1 2

99. TOT B-HCG Calibrator (CAL) II 3 Levels/3 Sets Box 2 4

100. TOT B-HCG II 100 Wells Box 7 12

101. Total Bilirubin (TBIL) Box/300 Slides Box 8 14

102. Total Protein 5 Pack/250 Slides Box 9 16

103. Total T Control (TOT T CNTL) 3 Levels/3 Sets Box 14 24

104. Total T4 100 Wells Box 6 10

105. Total T4 Calibrator (TOT T4 CAL) 3 Levels/1 Set Box 1 2

106. Troponin I ES 100 Wells Box 5 8

107. Troponin I ES Calibrator (CAL) 3 Levels/1 Set Box 1 2

108. Tryglycerides (TRIG) 5 Pack/300 Slides Box 8 14

109. TSH 100 Wells Box 19 32

110. TSH Calibrator 3 Levels/1 Set Box 2 4

111. UPRO Performance (PERF) VERIFIER I Box/6 Bottles Box 2 4

112. UPRO Performance (PERF) VERIFIER II Box/6 Bottles Box 2 4

113. Uric Acid (URIC) 5 Pack/300 Slides Box 4 6

114. Urine Chloride (CL-) 5 Pack/250 Slides Box 13 22

115. Urine Creatinine Control I Box 1 2

116. Urine Creatineine Control II Box 1 2

117. Urine Protein 5 Pack/90 Slides Box 2 4

118. Vancomycin Reagent (VANC) Box/300T Box 1 2

119. Vapor Adsorption Cartridge 1 Cartridge Box 2 4

120. VITROS VERSATIP Box/1000T Box 30 52

121. Wash Reagent Box/2 Bottles Box 5 8

122. %A1C Performance Verifier (PERF VER 1) 2 Levels/3 Vials Box 7 12

123. %A1C Performance Verifier (PERF VER II) 2 Levels/3 Vials Box 7 12

124. %emoglobin A1C Reagent 4 x 75 Tests Box 5 8

125. * IRON 5 Pack/90 Slides Box 5 8

126. ** XT ALB-TP Slide 5 Pack/250 Slides Box 6 11

127. ** XT ALTV-AST Slide 5 Pack/300 Slides Box 6 10

128. ** XT BUN/UREA-CREA Slide 5 Pack/300 Slides Box 6 10

129. ** XT GLUC-CA Slide 5 Pack/300 Slides Box 6 10

130. ** XT TBIL-ALKP Slide 5 Pack/300 Slides Box 5 8

131. ** XT TRIG-CHOL Slide 5 Pack/300 Slides Box 12 20

132. 800 Reference Fluids 30 Pouched Reservoirs Box 6 10

OPTION I PERIOD: 01 October 2019 – 30 September 2020

Reagent Unit Estimated Quantity

Maximum Quantity

1. Acetaminophone (ACET) 5 Pack/90 Slides Box 14 24

2. Anti-Hepatitis A Virus Immunoglobulin M (A-HAV IGM) 100 Wells Box 21 36

3. Anti-Hepatitis A Virus Immunoglobulin M Calibrator (A-HAV IGM CAL) 1 Level/1 Set

Box 6 10

4. Anti-Hepatitis A Virus Immunoglobulin M Control (A-HAV IGM CONTROL) 2 Levels/3 Sets

Box 14 24

5. Anti-Hepatitis A Virus (A-HAV) TOT 100 Wells Box 11 18

6. Anti-Hepatitis A Virus (A-HAV) Total Calibrator 1 Level/1 Vial Box 6 10

7. Anti-Hepatitis A Virus (A-HAV) Total Control 2 Levels/3 Sets Box 13 22

8. Anti-Hepatitis B Virus Core Antigen (ECI A-HBC) 100 Wells Box 25 42

9. Anti-Hepatitis B Virus Core Antigen (ECI A-HBC) Calibrator Box/1 Set Box 6 10

10. Anti-Hepatitis B Virus Core Antigen (ECI A-HBC) Control Box/3 Set Box 11 18

11. Anti-Hepatitis B Virus Surface Antigen (A-HBS) 100 Wells Box 21 36

12. Anti-Hepatitis B Virus Surface Antigen (A-HBS) Calibrator Box/1 Set Box 6 10

13. Anti-Hepatitis B Virus Surface Antigen (A-HBS) Control Box/3 Sets Box 14 24

14. Anti-Hepatitis C Virus (A-HCV) 100 Wells Box 25 42

15. Anti-Hepatitis C Virus Calibrator (A-HCV CAL) Box/1 Set Box 6 10

16. Anti-Hepatitis C Virus Control (A-HCV CNTL) Box/3 Set Box 11 18

17. Albumin (ALB) 5 Pack/250 Slides Box 32 54

18. Alcohol 5 Pack/90 Slides Box 18 30

19. Alkaline Phophatase (ALKP) 5 Pack/300 Slides Box 28 48

20. Alanine Aminotransferase (ALTV) 5 Pack/300 Slides Box 28 48

21. Amylase 5 Pack/90 Slides Box 14 24

22. Aspartate Aminotransferase (AST) 5 Pack/300 Slides Box 25 42

23. Bilirubin Unconjugated, Bilirubin Conjugated (BUBC) 5 Pack/90 Slides Box 18 30

24. Blood Urea Nitrogen (BUN) 5 Pack/300 Slides Box 25 42

25. Calcium (CA) 5 Pack/300 Slides Box 25 42

26. Calibrator Kit 1 3 Levels/4 Sets Box 2 4

27. Calibrator Kit 2 4 Levels/4 Sets Box 2 4

28. Calibrator Kit 3 3 Levels/4 Sets Box 2 4

29. Calibrator Kit 4 (ALB, BuBc, Fe, TBIL, TIBC, TOTAL PROTEIN) 4 Levels/4 Sets

Box 2 4

30. Calibrator Kit 5 (AMON, PROT) 3 Levels/4 Sets Box 1 2

31. Calibrator Kit 6 (CHE, CKMB) 3 Levels/4 Sets Box 1 2

32. Calibrator Kit 7 3 Levels/2 Sets Box 6 10

33. Calibrator Kit 8 3 Levels/2 Sets Box 2 4

34. Calibrator Kit 9 (ACET, CRBM, DGXN, PHBR, PHTY) 3 Levels/2 Sets Box 1 2

35. Calibrator Kit 10 3 Levels/2 Sets Box 2 4

36. Calibrator Kit 11 6 Levels/1 Set Box 2 4

37. Calibrator Kit 13 6 Levels/1 Set Box 2 4

38. Calibrator Kit 25 3 Levels/2 Sets Box 4 6

39. Calibrator Kit 31 4 Levels/3 Sets Box 4 6

40. Cerebrospinal Fluid (CSF) Protein 5 Pack/90 Slides Box 14 24

41. Cholesterol (CHOL) 5 Pack/300 Slides Box 25 42

42. Creatinine Kinase MB (CKMB) 5 Pack/90 Slides Box 13 22

43. CLINIQA Liquid QCTM Cardiac Marker Control (CLINIQA LIQ CARDIAC MKR CT VS) 1 Unit

Box 8 14

44. C-Reactive Protein (CRP) 5 Pack/90 Slides Box 35 60

45. C-Reactive Protein Performance (CRP PERF) VERIFIER I 2 Levels/6 Vials

Box 12 20

46. C-Reactive Protein Performance (CRP PERF) VERIFIER II 2 Levels/6

Box 12 20

47. Creatine Kinase (CK) 5 Pack/90 Slides Box 15 26

48. Creatinine/Isotope Diluation Mass Spectometry Standard (IDMS STD) 5 Pack/300 Slides

Box 28 48

49. DESICCANT PACKS Box/2 Sets Box 21 36

50. Diluent Pack 2 3 Packs Box 5 8

51. Diluent Pack 3 3 Packs Box 6 10

52. Direct High Density Lopoprotection (HDL) 5 Pack/300 Slides Box 32 54

53. Enzymatic CO2 (ECO2) 5 Pack/300 Slides Box 32 54

54. Free Thyroid Control (Free T Control) 3 Levels/3 Sets Box 21 36

55. Free T4 100 Wells Box 39 66

56. Free T4 Calibrator 3 Levels/3 Sets Box 6 10

57. FS Air Filter 1 Filter Box 2 4

58. FS CUVETTES Box/6000 Box 2 4

59. FS Humidifaction Packs 6 Packs Box 3 5

60. FS Micro Tip 4096 Tips Box 1 2

61. Gamma Glutamyl Transferase (GGT) 5 pack/250 Slides Box 14 24

62. Gentamicin Reagent (GENT) Box/300T Box 3 5

63. Glucose (GLU) 5 Pack/300 Slides Box 32 54

64. Hepatitis B Virus Antigen (JBSAG) 100 Wells Box 32 54

65. Hepatitis B Virus Antigen Calibrator (HBSAG CAL) Box/1 Vial Box 6 10

66. Hepatitis B Virus Antigen Control (HBSAG CNTL) Box/3 Sets Box 13 22

67. HI SAM DIL A (ON) 100WLS 1 Pack Box 11 18

68. HI SAM DIL B (ON) 100WLS 1 Pack Box 28 48

69. Immuno-Wash Fluid Box/30 Bottles Box 7 12

70. ISOENZYME Performance VERIFIER I (ISO PERF VERIFIER I) 2 Levels/6 Vials

Box 11 18

71. ISOENZYME Performance VERIFIER I (ISO PERF VERIFIER II) 2 Levels/6 Vials

Box 11 18

72. Lactate (LAC) 5 Pack/90 Slides Box 14 24

73. Lactate Dehydrogenase (Traceable to IFCC Reference Method) (LDHI) 5 Pack/250 Slides

Box 18 30

74. Lipase (LIP) 5 Pack/90 Slides Box 18 30

75. LIQUID Performance VERIFIER I (LIQ PERF VERIFIER I) 2 Levels/6 Vials

Box 14 24

76. LIQUID Performance VERIFIER II (LIQ PERF VERIFIER II) 2 Levels/6 Vials

Box 14 24

77. Magnesium (Mg) 5 Pack/300 Slides Box 13 22

78. Maintenance Pack Box/2 Packs Box 7 12

79. Micro Sample Cup 4000 Cups Box 14 24

80. MICROSNS CK FLS I&II Box/2 Sets Box 3 5

81. Perform Verifier I 2 Levels/12 Vials Box 14 24

82. Perform Verifier II 2 Levels/12 Vials Box 14 24

83. Phosphorus (PHOS) 5 Pack/300 Slides Box 8 14

84. Potassium (K+) 5 Pack/250 Slides Box 35 60

85. Reconstitution Diluent 12 Vials Box 2 4

86. Reflectometer Lamp 3 Box 7 12

87. REP ENDO CNTL 3 Levels/3 Sets Box 25 42

88. Rubella Immunoglobulin G (RUBELLA IGG) 100 Wells Box 11 18

89. Rubella Immunoglobulin G (RUBELLA IGG) Calibrator (CAL) 3 Levels/1 Set

Box 6 10

90. Salicylate 5 Pack/90 Slides Box 11 18

91. Sample Cup Pierceable Cap 1000 Caps Box 1 2

92. Signal Reagent Box/2 Packs Box 91 156

93. Sodium (NA+) 5 Pack/250 Slides Box 42 72

94. Therapeutic Drug Monitoring (TDM) PERF VERIFIER I 3 Levels/6 Vials Box 7 12

95. Therapeutic Drug Monitoring (TDM) PERF VERIFIER II 3 Levels/6 Vials Box 7 12

96. Therapeutic Drug Monitoring (TDM) PERF VERIFIER III 3 Levels/6 Vials

Box 7 12

97. TORCH Negative Control Box 2 4

98. TORCH Positive Control Box 2 4

99. TOT B-HCG Calibrator (CAL) II 3 Levels/3 Sets Box 6 10

100. TOT B-HCG II 100 Wells Box 21 36

101. Total Bilirubin (TBIL) Box/300 Slides Box 25 42

102. Total Protein 5 Pack/250 Slides Box 28 48

103. Total T Control (TOT T CNTL) 3 Levels/3 Sets Box 42 72

104. Total T4 100 Wells Box 18 30

105. Total T4 Calibrator (TOT T4 CAL) 3 Levels/1 Set Box 4 6

106. Troponin I ES 100 Wells Box 14 24

107. Troponin I ES Calibrator (CAL) 3 Levels/1 Set Box 4 6

108. Tryglycerides (TRIG) 5 Pack/300 Slides Box 25 42

109. TSH 100 Wells Box 56 96

110. TSH Calibrator 3 Levels/1 Set Box 7 12

111. UPRO Performance (PERF) VERIFIER I Box/6 Bottles Box 7 12

112. UPRO Performance (PERF) VERIFIER II Box/6 Bottles Box 7 12

113. Uric Acid (URIC) 5 Pack/300 Slides Box 11 18

114. Urine Chloride (CL-) 5 Pack/250 Slides Box 39 66

115. Urine Creatinine Control I Box 1 2

116. Urine Creatineine Control II Box 1 2

117. Urine Protein 5 Pack/90 Slides Box 7 12

118. Vancomycin Reagent (VANC) Box/300T Box 4 6

119. Vapor Adsorption Cartridge 1 Cartridge Box 6 10

120. VITROS VERSATIP Box/1000T Box 91 156

121. Wash Reagent Box/2 Bottles Box 14 24

122. %A1C Performance Verifier (PERF VER 1) 2 Levels/3 Vials Box 21 36

123. %A1C Performance Verifier (PERF VER II) 2 Levels/3 Vials Box 21 36

124. %emoglobin A1C Reagent 4 x 75 Tests Box 14 24

125. * IRON 5 Pack/90 Slides Box 14 24

126. ** XT ALB-TP Slide 5 Pack/250 Slides Box 20 34

127. ** XT ALTV-AST Slide 5 Pack/300 Slides Box 16 28

128. ** XT BUN/UREA-CREA Slide 5 Pack/300 Slides Box 16 28

129. ** XT GLUC-CA Slide 5 Pack/300 Slides Box 16 28

130. ** XT TBIL-ALKP Slide 5 Pack/300 Slides Box 14 24

131. ** XT TRIG-CHOL Slide 5 Pack/300 Slides Box 29 49

132. 800 Reference Fluids 30 Pouched Reservoirs Box 18 30

OPTION II PERIOD: 01 October 2020 – 30 September 2021

Quantity