| Primary Device ID | 10709078004794 |
| NIH Device Record Key | e32dc283-5caf-4367-97c1-5ef1684b2f8c |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Transpot Kit with Oxygen Mask |
| Version Model Number | 9440 |
| Company DUNS | 092673953 |
| Company Name | WESTMED, INC. |
| 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 | true |
| Device Combination Product | false |
| Single Use | true |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | false |
| Expiration Date | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | true |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00709078004797 [Primary] |
| GS1 | 10709078004794 [Package] Contains: 00709078004797 Package: [25 Units] In Commercial Distribution |
| OGL | Oxygen Administration Kit |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2018-06-18 |
| Device Publish Date | 2018-05-16 |
| 10709078000574 - VixOne | 2025-12-02 Small Volume Nebulizer |
| 00709078049996 - Filter | 2025-10-01 Entered in error |
| 00709078050008 - Filter | 2025-10-01 Entered in error |
| 10709078008402 - Flex Extenders | 2024-10-03 Flex Extender, 5.2" x 15mm OD x 22/15mm ID |
| 20889483562786 - Disposable Anesthesia Breathing Circuit | 2024-09-16 Breathing Circuit, Pediatric, 60", Parallel Wye w/Port |
| 20889483612009 - Anesthesia Circuit Kit | 2024-06-10 60" Adult Anesthesia Circuit; Swivel Wye, 2L LF Bag |
| 20889483612016 - Anesthesia Circuit Kit | 2024-06-10 60" Adult Anes. Circuit; Par-Wye, GSE, 2L Latex Free |
| 20889483612023 - Anesthesia Circuit Kit | 2024-06-10 60" Pediatric Anes. Circuit, Par-Wye, GSE W/Port |