PD_Rev0_16M_207A_MA_Pipette_Balance.docx
DOCX document 31 KB Posted
- Attached to
- Pipette Balance Federal contract opportunity
- Solicitation number
- FA2263-16-Q-0007
About this file
Purchase Description 207A
View the file
Other files for this federal contract opportunity
| File | Type | Posted |
|---|---|---|
| PD_Attachment_Data_Requirements.docx | DOCX document | |
| DIDS.pdf | ||
| Anticipated_Delivery_Locations_207A.doc | DOC document | |
| Schedule_B_207A.docx | DOCX document | |
| Signed_1423_207A.pdf |
On GovTribe
Work with this file on GovTribe
- Download the original file
- Contacts named in this file
- Similar government files
- Ask GovTribe AI about this file
Text version
16M-207A-MA
24 June 2015 Rev 0
PURCHASE DESCRIPTION
FOR
Pipette Balance
1.0 SCOPE: This purchase description specifies a Pipette Balance to be used in the calibration of pipettes by selected Precision Measurement Equipment Laboratories (PMELs) in the range of 0 to 100 grams.
2.0 PERFORMANCE REQUIREMENTS:
2.1 Display Resolution: The Pipette Balance shall be readable to 0.001 mg for the range 0 to 22 g and 0.01 mg from 22 g to 100 g.
2.2 Measuring Range: The Pipette Balance shall have a measuring range which covers 0 to 100 grams minimum. More than one balance may be required to meet this measuring range and accuracies associated with them.
2.3 Repeatability: The repeatability of the instrument shall be 0.0025 mg for the range 0 to 22 g and 0.05 mg from 22 g to 100 g.
2.4 Reliability: Item shall maintain its repeatability specification over a period of 12 months, minimum.
2.5 Eccentricity: The eccentricity of the instrument shall not exceed 0.025 mg for the range of 0 to 22 g and 0.4 mg from 22 g to 100 g.
2.6 Linearity: The linearity of the instrument shall not exceed 0.01 mg for the range of 0 to 22 g and 0.15 mg from 22 to 100 g.
2.7 Stabilization Time: The stabilization time for an individual reading shall be no more than 20 seconds.
3.0 FUNCTIONAL REQUIREMENTS:
3.1 Multi-Channel Workstation: This shall be included with the range of 0 to 100 g. It shall be capable of holding 12 pipettes at the same time.
4.0 MECHANICAL & PHYSICAL REQUIREMENTS:
4.1 Components: Commercial parts and materials that are used shall have properties consistent with a precision laboratory instrument.
4.2 Use of Best Commercial Practices: The equipment shall be designed and constructed of materials that meet the requirements of this specification and in accordance with the best commercial practices for industry approved equipment. It shall be designed and manufactured to maximize reliability, maintainability, accuracy of operation, and ease of operation. All parts (which include, but are not limited to, shafts, bearings, regulators, switches, controls) shall have proper clearance and adjustments. They shall work together so that the equipment will supply the rated requirements without unnecessary strains, vibrations or overheating. They shall be able to withstand the conditions met in shipping, storage, installation and service. All materials and parts of this equipment shall be capable of withstanding the environmental requirements of this specification.
4.3 Matched and Selected Components: These shall be kept to an absolute minimum. Use of specially built, nonstandard components shall be avoided.
4.4 Model and Serial Number Identification: Item’s Part Number, Manufacturer, and Serial Number shall be identified clearly on the item in a location visible to the operator. Unique item identification shall follow the Item Identification and Valuation clause as stated in the contract.
4.5 Operating Environment/Storage:
4.5.1 Operating Temperature: Electrical, electronic, and electromechanical items shall be capable of operating in an ambient temperature of 67 to 79 degrees F without loss of required performance.
4.5.2 Operating Humidity: The equipment shall maintain specified performance in an atmosphere from 20% to 50% relative humidity without loss of required performance.
4.6 Facility Electrical Power and Connections: The Mass Comparator shall be capable of operating on standard 110 V AC 60 Hz electrical power.
4.7 Safety: Documentation will be provided to support the means by which electrical safety considerations have been addressed. The safety of all personnel will be assured in conductive or nonconductive contact with the outside of the equipment, and during the changing of the fuse with the power to the system and its components are turned on. This documentation shall consist of a minimum of a citation of a UL or ANSI identified standard or equivalent United States Standard that the equipment conforms to.
5.0 CONTROLLER REQUIREMENTS:
A laptop controller is required that can efficiently operate under Microsoft Windows 7 Professional operating system. All major components of the system must be commercially available and fully supportable by commercial sources. Where specific brands are identified in this specification, no substitutes are allowed without prior approval from AFMETCAL. The Controller must meet or exceed Microsoft Windows 7 Professional hardware requirements.
5.1 Processor: Intel Pentium IV or otherwise equivalent or better generation minimum, 1 GHz clock speed minimum.
5.2 Memory: Minimum 4 GB system Memory.
5.3 Input Output (I/O) External Ports, Slots and Connectors:
At minimum, the following types of I/O interface connections must be available on the controller or via port replication:
5.3.1 USB: Minimum of four integrated USB Ver 2.0 compliant ports.
5.3.2 Ethernet: One 100/1000 BaseT Ethernet RJ45 port.
5.3.3 Video: Areo-Capable Graphics card that supports Windows Display Driver Model (WDDM 1.0) with a minimum of 128 MB.
5.4 Display Panel: Minimum 15-inch LCD Color Display Panel with at least 1024 x 768 resolution for a 4:3 aspect ratio or 14.1-inch flat panel LCD Color Display Panel with at least 1280 x 720 resolution for a 16:9 aspect ratio.
5.5 Hard Drive: 80 GB (Minimum) Hard Disk Drive.
5.6 DVD-ROM/CD-RW Drive
DVD-R: at least 8X Speed CD-RW: at least 24X Read Speed, 16x Write Speed
5.7 Operating System and Software: All software shall run under or Microsoft Windows7 (Professional operating system or greater, 64 bit, latest version release). All software shall run Windows 7 as a non-elevated user.
5.8 Additional Hardware: Additional hardware required to make this system function as identified by this purchase description shall be provided.
5.9 Software: Software shall be provided for the application of calibrating pipettes and other dispensing systems for liquids in the range of 0.1 l to 100 ml. It shall be operated using Microsoft Windows 7 as a non-elevated user.
5.9.1 Pipette: The software shall allow the user to add in new pipettes by serial number and part number.
5.9.2 Range: The software shall allow the user to select the measuring range of the pipette.
5.9.3 Environmental Conditions: The software shall allow the user to input the environmental conditions or be capable of extracting that information from an external data source automatically.
5.9.4 Calibrating Pipettes: The software shall lead the user through defined steps and record the data points automatically for both single and multi-channel pipettes.
5.9.5 Calibration Reports: The software shall be capable of printing calibration reports with all the recorded data points along with pass/fail identification. The report shall also include the user input identification of the pipette being calibrated.
6.0 Training: Training shall be provided for up to four people not to exceed two days. Training will consist of operation and use of the system, including all software functions.
7.0 TESTING: This item will be inspected and accepted at destination as stated in the contract. The item will be checked with test equipment with parameters equal to or better than those required to assure that specified performance parameters are met. Test equipment used shall have first echelon certification directly traceable to the National Institute of Standards Technology (NIST) or other AFMETCAL-approved equivalent international laboratory. Tests will be performed to assure that the item meets the requirements of this purchase description. Such testing at destination does not relieve the contractor of performing all inspections and quality checks at the point of manufacture as necessary to assure performance as specified herein.
Attachment 1. Data Requirements
File details come from the government source that posted it. Updated .