- Physicians Office Resource

The VITEK® 2 ANC Identification Card is intended for use with the VITEK 2 Systems for ID of clinically important anaerobic bacteria and coryneform bacteria
VITEK® 2 ANC - VITEK® 2 ANC

Device Description

A collection of reagents and other associated materials intended to be used for the differentiation and/or identification of one or multiple species of anaerobic bacteria isolated by culture from a clinical specimen.

Environmental Conditions

Storage Environment Temperature - Degrees Celsius

8.00
2.00

Device Sizes

No Data Available

Device Sterilization

Device Sterile: False

Sterilization Prior To Use: False

Sterilization Methods: No Data Available

Product Codes

Code: JSP

Device Name: Kit, Anaerobic Identification

Device Class: 1

Physical State: N/A

Definition: N/A

Submission Type ID: 4

Review Panel: MI

Review Code: N/A

Technical Method: N

Gmp Exempt Flag: N/A

Life Sustain Support Flag: N

Unclassified Reason: N/A

Implant Flag: N

Target Area: N/A

Regulation Number: 866.2660

Third Party Flag: N

Medical Specialty: MI

Device Identifiers

Device Id: 03573026144364

Device Type: Package

DeviceId Issuing Agency: GS1

Contains DI Number: 03573026529727

Package Quantity: 20

Package Discontinue Date: N/A

Package Status: In Commercial Distribution

Package Type: N/A

Device Id: 03573026529727

Device Type: Primary

DeviceId Issuing Agency: GS1

Contains DI Number: N/A

Package Quantity: N/A

Package Discontinue Date: N/A

Package Status: N/A

Package Type: N/A

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