| Primary Device ID | 10886705008186 |
| NIH Device Record Key | 30d2ff4b-d3f9-45a9-a3fc-250d4fbdb680 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | HEALIX TRANSTEND |
| Version Model Number | 222273 |
| Catalog Number | 222273 |
| Company DUNS | 190572854 |
| Company Name | DEPUY MITEK, LLC |
| 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 | false |
| 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 | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 10886705008186 [Primary] |
| LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[10886705008186]
Moist Heat or Steam Sterilization
[10886705008186]
Moist Heat or Steam Sterilization
[10886705008186]
Moist Heat or Steam Sterilization
[10886705008186]
Moist Heat or Steam Sterilization
[10886705008186]
Moist Heat or Steam Sterilization
[10886705008186]
Moist Heat or Steam Sterilization
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2022-06-10 |
| Device Publish Date | 2015-09-01 |
| 10886705020331 | HEALIX TRANSTEND Drill Bit 2.2mm |
| 10886705008186 | HEALIX TRANSTEND 3.4mm Awl/Tap |
| 10886705023868 | 222341 |