Primary Device ID | 05032384104659 |
NIH Device Record Key | 2cbd137a-53c6-4ee3-9048-956ef9f2f7ea |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | V FACTOR |
Version Model Number | DD0004B |
Company DUNS | 365355452 |
Company Name | OXOID LIMITED |
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 | 05032384104659 [Primary] |
JTO | Discs, Strips And Reagents, Microorganism Differentiation |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-12-12 |
Device Publish Date | 2022-12-04 |
05032384104659 | DD0004B |
05032384034079 | DD0004T |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
V FACTOR 78826410 not registered Dead/Abandoned |
Mazzotta, Paul F. 2006-03-01 |