Primary Device ID | 04015630938872 |
NIH Device Record Key | 4f8d898c-2750-4ce3-a612-c2a78b89e1c5 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | PreciControl Anti-HBe |
Version Model Number | 11876384160 |
Catalog Number | 11876384160 |
Company DUNS | 315028860 |
Company Name | Roche Diagnostics GmbH |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | Labeling does not contain MRI Safety Information |
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 | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 04015630938872 [Primary] |
LOM | Test, Hepatitis B (B Core, Be Antigen, Be Antibody, B Core Igm) |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2021-04-15 |
Device Publish Date | 2021-04-07 |
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