| 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 |