| Primary Device ID | 00848838022371 |
| NIH Device Record Key | 2c2c7e6b-b300-43f6-af2f-291928eb3f4f |
| Commercial Distribution Status | In Commercial Distribution |
| Version Model Number | R21090 |
| Company DUNS | 065769564 |
| Company Name | REMEL, INC. |
| Device Count | 25 |
| 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 | true |
| 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 |
| Phone | 8002556730 |
| ITechnicalSupport@remel.com |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00848838022371 [Primary] |
| GS1 | 00848838099809 [Unit of Use] |
| MJD | Culture Media, Antimycobacteria, Susceptibility Test |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2018-03-29 |
| Device Publish Date | 2016-12-09 |
| 00848838072529 - RapID | 2025-05-06 RapID STAPH PLUS QC Set/4 |
| 00848838023156 - REMEL | 2025-04-02 Anaer Nitrate Reagent A BTL/25ml |
| 00848838023194 - REMEL | 2025-04-02 Bile Solubility Reagent (2%) BTL/25ml |
| 00848838023200 - REMEL | 2025-04-02 Anaer Nitrate Reagent B BTL/25ml |
| 00848838023385 - REMEL | 2025-04-02 Nitrate Reagent A for AFB BTL/25ml |
| 00848838023392 - REMEL | 2025-04-02 Nitrate Reagent B for AFB BTL/25ml |
| 00848838023606 - REMEL | 2025-04-02 PS80 Hydrolysis Substrate Conc VL/5ml |
| 00848838031205 - REMEL | 2025-04-02 Malachite Green (5%) BTL/250ml |