Primary Device ID | 05032384184835 |
NIH Device Record Key | 525c78b9-fa02-4cc8-93d8-d629bc2a3d02 |
Commercial Distribution Status | In Commercial Distribution |
Version Model Number | CT1895B |
Company DUNS | 365355452 |
Company Name | OXOID LIMITED |
Device Count | 5 |
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 |