| Primary Device ID | 00840117323315 |
| NIH Device Record Key | 86c43ba2-0613-4234-bda4-1b489591ce28 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Resp-O2 Nasopharyngeal Airways, 22 FR |
| Version Model Number | 36276 |
| Company DUNS | 008124539 |
| Company Name | DYNAREX CORPORATION |
| 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 | false |
| Serial Number | false |
| Manufacturing Date | false |
| 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 | 00840117315297 [Package] Contains: 00840117315389 Package: Master Shipper [10 Units] In Commercial Distribution |
| GS1 | 00840117315389 [Package] Package: Case [10 Units] In Commercial Distribution |
| GS1 | 00840117323315 [Primary] |
| BTQ | Airway, Nasopharyngeal |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2022-05-26 |
| Device Publish Date | 2022-05-18 |