Primary Device ID | 05032384519828 |
NIH Device Record Key | 37c66e2b-d531-4605-9460-3a49e845c403 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | ProSpecT™ Wash Buffer |
Version Model Number | R2450001 |
Company DUNS | 365355452 |
Company Name | OXOID LIMITED |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
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 | 05032384519828 [Primary] |
LLH | Reagents, Clostridium Difficile Toxin |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-07-15 |
Device Publish Date | 2024-07-05 |