| Primary Device ID | 00840117317376 |
| NIH Device Record Key | ff511e10-aaeb-4af6-bd7e-9fac41bb9fd1 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Resp-O2 Endotracheal Tube, Uncuffed, 5.0 mm |
| Version Model Number | 36226 |
| Company DUNS | 008124539 |
| Company Name | DYNAREX CORPORATION |
| Device Count | 1 |
| 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 | 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 | 00840117312746 [Package] Package: Box [10 Units] In Commercial Distribution |
| GS1 | 00840117312753 [Package] Contains: 00840117312746 Package: Case [10 Units] In Commercial Distribution |
| GS1 | 00840117317376 [Primary] |
| BTR | Tube, Tracheal (W/Wo Connector) |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2022-05-23 |
| Device Publish Date | 2022-05-15 |