| Primary Device ID | 20643169060849 |
| NIH Device Record Key | 212c6276-e0d9-4cf0-8afb-b79b2bfd3840 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | TriVantage™ |
| Version Model Number | 8229737 |
| Company DUNS | 835465063 |
| Company Name | MEDTRONIC XOMED, INC. |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | MR Unsafe |
| 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 | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | true |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com |
| Lumen/Inner Diameter | 7 Millimeter |
| Lumen/Inner Diameter | 7 Millimeter |
| Lumen/Inner Diameter | 7 Millimeter |
| Lumen/Inner Diameter | 7 Millimeter |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00643169060845 [Primary] |
| GS1 | 20643169060849 [Package] Contains: 00643169060845 Package: PK [3 Units] In Commercial Distribution |
| ETN | STIMULATOR, NERVE |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2016-04-22 |
| 20643169060863 | EMG TUBE 8229739 3PK NIM TRIVANTAGE 9MM |
| 20643169060856 | EMG TUBE 8229738 3PK NIM TRIVANTAGE 8MM |
| 20643169060849 | EMG TUBE 8229737 3PK NIM TRIVANTAGE 7MM |
| 20643169060832 | EMG TUBE 8229736 3PK NIM TRIVANTAGE 6MM |
| 20643169060825 | EMG TUBE 8229735 3PK NIM TRIVANTAGE 5MM |