Primary Device ID | 07613336156551 |
NIH Device Record Key | bbe5a573-f5d0-4f82-a9c3-c0a1ebb0243a |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | cobas Liat Influenza AB Script Version 1.33 |
Version Model Number | 08403864001 |
Catalog Number | 08403864001 |
Company DUNS | 071674100 |
Company Name | Roche Molecular Systems, Inc. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | MR Safe |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | false |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 07613336156551 [Primary] |
OOI | real time Nucleic acid amplification system |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2018-03-29 |
Device Publish Date | 2017-11-17 |
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