RFQ 75N91024Q00124 - SON.pdf

STATEMENT OF NEED (SON)

75N91024Q00124 Page 1 of 5 National Institutes of Health / National Cancer Institute / Office of Acquisitions

1.0 TITLE

Procurement of One (1) Brand Name or Equal Steris AMSCO 250LS Small Steam Sterilizer and Associated Equipment

2.0 BACKGROUND

The National Cancer Institute (NCI), Center for Cancer Research’s (CCR), Laboratory of Cell Biology (LCB) is engaged in a variety of research areas including drug resistance in cancer, drug transporters, p53, RNA metabolism and epitranscriptomics, and cancer metastasis. LCB currently uses a Steris autoclave that has reached the end of its useful life and must be replaced. The autoclave is used to sterilize equipment and materials critical for aseptic conditions and for conducting animal and zebrafish experiments in compliance with Association for Assessment and Accreditation of Laboratory Animal Care (AAALAC) and Institutional animal care and use committee sterility regulations.

LCB seeks a replacement autoclave that fits in the same space in the lab and matches the existing plugs.

Therefore, LCB requires one (1) Brand Name or Equal Steris AMSCO 250LS Small Steam Sterilizer and associated equipment listed in Section 4.0 below.

3.0 TYPE OF ORDER

This shall be a Firm Fixed-Price Purchase Order.

4.0 SPECIAL ORDER REQUIREMENTS

ITEM DESCRIPTION QTY UNIT

1 Brand Name or Equal AMSCO 250LS Small Steam Sterilizer w/ Loading Rack & Two Shelves. Installation & Deinstallation services.

1 EA

2 Brand Name or Equal Intermediate Shelf for AMSCO 250LS Small Steam Sterilizer

1 EA

3 Brand Name or Equal AMSCO Base Spare Parts Package for AMSCO 250 Sterilizer

1 EA

NOTE: NCI will not be responsible for any shipping charges not listed in the quotation.

4.1 PRODUCT FEATURES/SALIENT CHARACTERISTICS

The following product features/characteristics are required for this equipment:

1. Footprint:

Due to space limitations, the autoclave must have a compact footprint:

a. Dimensions not to exceed 20 x 20 x 38 inches (508 x 508 x965mm)

b. Storage capacity of at least 250 ml

2. Control system:

a. The autoclave shall have an Allen Bradley MicroLogix Panel View Plus 600 interface screen

b. The autoclave shall have a touch sensitive screen with 18-bit color graphic.

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c. The autoclave shall have a copy display that has a 640 x 480 resolution color active matrix.

d. The autoclave shall a display designed with emphasis on human factors and user recognizable symbols.

3. Standards and Governing Directives:

a. The autoclave shall meet the requirements of the following listings and standards:

i. Low voltage directive (2014/35/EU, EMC Directive (2014/30/EU and Machinery Directive (2006/42/EEC)

ii. Pressure Equipment Directive (PED): 97/23/EC

iii. UL/EN/CSA 61010-1: Safety requirements for electrical equipment

iv. UL/EN/CSA/61010-2-040: Safety requirements for sterilizers used to treat medical materials

v. ASME Code, Section VIII, Division 1: unfired pressure vessels door and shell can withstand a working pressure of 45psig (3.1 bar)

4. Operational Cycles:

a. The autoclave shall include the following operational cycles:

i. Gravity Cycle: prevacuum for sterilization of moisture stable goods at 100C to 141 C and decontamination of bagged non-bio-hazardous lab wastes

ii. Liquid Cycle: Sterilization of liquid and media at 100 C to 141C using cooling feature to control exhaust rate

iii. Prevacuum Cycle: High volume sterilization for heat and porous materials at 100C to 141C utilizing a mechanical air evacuation

iv. USP 660 Cycle: sterilization cycle for glassware

v. Continuous Cycle: Cycle for up to 9999 cycles to be run consecutively without the need of an operator

vi. Waste bag Cycle: cycle effective for processing lab waste in autoclave bags

vii. Leak Test Cycle: verification of door seal and piping system integrity

b. The autoclave must have a Display System that includes:

i. 20 cycles that can be individually selected and programmed

ii. Help screens for control operation

iii. Program that can be permanently stored in flash memory

iv. Variables that can be permanently stored in flash memory

5. Safety features:

a. The autoclave must have the specified safety features:

i. Control lockout switch

ii. Chamber float switch

iii. Pressure relief valve

iv. Emergency stop button

6. Energy Savings:

a. The autoclave shall be environmentally sustainable with:

i. Automatic utilities Startup/Shutdown: Shuts off all utility valves when activated to conserve steam and water usage

ii. Green Mode: shut off steam to unit if idle for a specified time

iii. Green Gravity water saver system: collection of steam effluent to reduce water usage

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7. Autoclave construction:

a. The autoclave shall have a chamber system to include the following:

i. Sterilizer vessel that is ASME rated at 50psig (3.2 Bar) and insulated

ii. Chamber door that is steam-activated during cycle operation

iii. Chain drain system that is designed to prevent pollutants from entering the building water supply system and sterilizer

iv. Automatic drain effluent cooling

b. The autoclave shall have a vacuum system were the conditioning and drying phase is reduced by a standard water ejector

c. The autoclave shall have a steam source that is piped, valved, and trapped to receive building steam delivered at 50 to 80 psig

d. The autoclave shall have piping and connections that terminate with the confines of the sterilizer and include:

I. Accessibility form the front and side of sterilizer

ii. solenoid valves in manifold that can be serviced individually

iii. manual shutoff valves that are pressure rated at 125 psig

8. The autoclave shall have the following standard features:

a. Hinged front cabinet panel

b. Resistance Temperature detectors (RTDs): Provide sterilizer temperature control

c. Software calibration: available for all temperature and pressure inputs

d. Cycle data records: recorded on tape or for onscreen review

e. Optimum solution cooling

f. Steam purge: Assists in air removal and preheating the load

g. Automatic stem shutoff to jacket

h. Insulation: one-inch-thick asbestos free spin glass (rated at 1000F/538C

g. Lighted DIN connectors: Installed on steam, water, and exhaust valves

h. Air backup: Provided with bioseals or air differential seals

i. Visible gauges: Chamber and jacket pressure gauges

9. Warranty of fifteen years for pressure vessel with parts and labor and two years for door seal.

4.2 WARRANTY

In addition to the Implied warranty contained in FAR Clause 52.212-4, the Contractor is encouraged to provide express warranties. At a minimum, the Contractor shall provide a 12-month warranty from date of final installation on all equipment and associated items provided under, or as a part of this purchase order.

The warranty shall include repair and or replacement of parts, including travel, labor, and materials, at no additional cost to the Government. The warranty shall not exclude or limit the Governments rights for an Implied warranty as established in the terms and conditions of clause 52.212-4.

4.3 DELIVERY / INSTALLATION

Delivery shall be within six (6) weeks of the purchase order award. All shipping/handling (including FOB Destination) and delivery/installation fees shall be included in the quote. Upon delivery, the Contractor shall notify the respective NCI Technical Point of Contact to schedule installation dates and times. Installation shall occur within fourteen (14) calendar days of delivery and shall be performed by, or under the direct supervision of, a certified operator.

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The contractor shall deliver and install the equipment at the following address:

Laboratory of Cell Biology, National Institutes of Health/NCI 9000 Rockville Pike Bethesda, MD 20892 Technical Point of Contact: [to be provided upon award]

4.3.1 DELIVERY GUIDANCE

The Contractors shall communicate and follow instructions from the Technical Point of Contact (TPOC) to coordinate delivery and installation.

The Contractor shall direct all courier and delivery services – including those not operated by the Contractor (e.g. FedEx, USPS, UPS) – to follow the instructions in this section.

All companies delivering to the NIH main campus must comply with Commercial Vehicle Inspection Facility (CVIF) access procedures. Upon arrival, the CVIF will provide a list of buildings and loading docks to delivery personnel.

Deliveries will be logged in at the loading dock, and the loading dock contractor or Government personnel will attempt to contact the TPOC listed on the package. In the event that the TPOC is unable to accept the package, the delivery shall not be left at the loading dock station. The delivery must be returned to the Contractor, and the Contractor must coordinate with the TPOC to deliver on another date at no additional cost.

Deliveries can only be made between 6:00 a.m. and 4:00 p.m. EST, Monday – Friday, excluding federal holidays.

4.4 INSPECTION AND ACCEPTANCE

Pursuant to FAR Clause 52.212-4, all items to be delivered in relation to this Purchase Order are subject to final inspection and acceptance by an authorized representative of the Government. The authorized representative of the Government is the TPOC who is responsible for inspection and acceptance of all services, materials, or supplies to be provided by the Contractor.

The TPOC has limited authority as defined within this Statement of Need. They do not have the authority to commit or obligate Government funds or make changes to the terms and conditions of the purchase order. As such, any changes to the purchase order must be performed by a warranted Government Contracting Officer with appropriate delegated authority to do so.

4.5 TRAINING

The Contractor shall provide on-site training at the laboratory in which equipment is installed (See Section 4.3). The provided training shall be for one (1) day and accommodate a minimum of eight (8) staff. This training shall be conducted within seven (7) calendar days after equipment installation in the designated laboratory. Training shall be conducted by a certified operator. The user training shall include an overview of setup approaches, instrument settings, and a demonstration of the performance. Instrument care and maintenance must also be covered and information about

75N91024Q00124 Page 5 of 5 accessing unlimited technical support. All training expenses, including materials and or travel expenses shall be included in the quoted price.

5.0 PAYMENT

Payment shall be made in full after the successful delivery, installation, training, and acceptance of equipment by the NCI Technical Point of Contact (TPOC). Payment authorization requires submission and approval of invoices to the NCI TPOC and NIH OFM.