| Primary Device ID | 05023323000491 |
| NIH Device Record Key | faa6fa36-16d4-419d-bf2f-be757f59eac1 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Clement Clarke International |
| Version Model Number | 3122064 |
| Company DUNS | 216155952 |
| Company Name | CLEMENT CLARKE INTERNATIONAL 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 | true |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | true |
| Expiration Date | false |
| 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 | 05023323000491 [Package] Contains: 05023323029478 Package: [200 Units] In Commercial Distribution |
| GS1 | 05023323029478 [Primary] |
| BYP | Mouthpiece, Breathing |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2022-12-13 |
| Device Publish Date | 2022-12-05 |
| 05023323029515 | UNIVERSAL M/PIECES IN BAG X15 |
| 05023323029492 | O:W:VAL:PAED:M/PCE:ADAPT:PK 20 |
| 05023323001344 | ONE WAY VALVE EXP (500) |
| 05023323000491 | ONE WAY VALVE EXP (200) |
| 05023323000507 | ONE WAY VALVE INSPIRATORY (200) |
| 05023323001559 | ONE WAY VALVE: EXP (5X20) |
| 05023323001191 | ONE WAY VALVE INSP (500) |
| 05023323001085 | ONE WAY VALVE INSPIRATORY (5X20) |