DEVICE: Alere i Influenza A & B 2 (10811877010019)
Device Identifier (DI) Information
Alere i Influenza A & B 2
427-000
Not in Commercial Distribution
Alere Scarborough, Inc.
427-000
Not in Commercial Distribution
Alere Scarborough, Inc.
A rapid, automated, molecular test for the qualitative detection of influenza A and B viral nucleic acid in respiratory specimens.
Device Characteristics
| Labeling does not contain MRI Safety Information | |
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GMDN
[?]GMDN© Term Code, Names and Definitions (*Terms of Use): GMDN® is a registered trademark of The GMDN Agency. All rights reserved. Used under licence from The GMDN Agency Ltd.
| GMDN Term Code | GMDN Term Name | GMDN Term Definition | GMDN Term Status [?] | Implantable? |
|---|---|---|---|---|
| 47277 | Influenza A/B virus nucleic acid IVD, kit, nucleic acid technique (NAT) |
A collection of reagents and other associated materials intended to be used for the qualitative and/or quantitative detection of nucleic acid from influenza A virus and/or influenza B virus in a clinical specimen, using a nucleic acid technique (NAT).
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FDA Product Code
[?]| Product Code | Product Code Name |
|---|---|
| OCC | Respiratory Virus Panel Nucleic Acid Assay System |
| OZE | Influenza A And Influenza B Multiplex Nucleic Acid Assay |
| OOI | Real Time Nucleic Acid Amplification System |
FDA Premarket Submission
| FDA Premarket Submission Number [?] | Supplement Number [?] |
|---|---|
| K171792 | 000 |
Sterilization
Storage and Handling
[?]| Storage and Handling |
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| No storage/handling found |
Clinically Relevant Size
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| No Device Sizes |
Device Record Status
920d9dfd-8f57-4a5c-8cf8-395d7ef7d8bf
September 12, 2023
3
November 20, 2017
September 12, 2023
3
November 20, 2017
Alternative and Additional Identifiers Additional Identifiers
Package DI
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Secondary DI
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| No Secondary DIs found | |
Unit of Use DI
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Unit of Use DI Number:
No Unit of Use DI Numbers Found
CLOSE
Direct Marking (DM)
[?]Production Identifier(s) in UDI
[?]Customer Contact
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No Customer Contact currently defined