| Primary Device ID | 00880304373013 |
| NIH Device Record Key | 99a88031-d004-48af-9428-2cc58b05342c |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | ULTRA-DRIVE |
| Version Model Number | 423874 |
| Catalog Number | 423874 |
| Company DUNS | 129278169 |
| Company Name | Biomet Orthopedics, LLC |
| 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 | true |
| Serial Number | false |
| Manufacturing Date | false |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Phone | 1-800-348-9500 |
| customerservice@biomet.com | |
| Phone | 1-800-348-9500 |
| customerservice@biomet.com | |
| Phone | 1-800-348-9500 |
| customerservice@biomet.com | |
| Phone | 1-800-348-9500 |
| customerservice@biomet.com | |
| Phone | 1-800-348-9500 |
| customerservice@biomet.com | |
| Phone | 1-800-348-9500 |
| customerservice@biomet.com | |
| Phone | 1-800-348-9500 |
| customerservice@biomet.com | |
| Phone | 1-800-348-9500 |
| customerservice@biomet.com | |
| Phone | 1-800-348-9500 |
| customerservice@biomet.com | |
| Phone | 1-800-348-9500 |
| customerservice@biomet.com | |
| Phone | 1-800-348-9500 |
| customerservice@biomet.com | |
| Phone | 1-800-348-9500 |
| customerservice@biomet.com | |
| Phone | 1-800-348-9500 |
| customerservice@biomet.com | |
| Phone | 1-800-348-9500 |
| customerservice@biomet.com | |
| Phone | 1-800-348-9500 |
| customerservice@biomet.com | |
| Phone | 1-800-348-9500 |
| customerservice@biomet.com |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00880304373013 [Primary] |
| JXE | Device, Nerve Conduction Velocity Measurement |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 4 |
| Public Version Date | 2018-07-24 |
| Device Publish Date | 2016-10-03 |
| 00880304858992 - JUGGERKNOT | 2025-09-22 |
| 00880304404809 - MINI RC NEEDLE | 2025-09-08 |
| 00887868571718 - RingLoc®+ Triflange | 2025-06-20 |
| 00887868571725 - RingLoc®+ Triflange | 2025-06-20 |
| 00887868571732 - RingLoc®+ Triflange | 2025-06-20 |
| 00887868571749 - RingLoc®+ Triflange | 2025-06-20 |
| 00887868571756 - RingLoc®+ Triflange | 2025-06-20 |
| 00887868571763 - RingLoc®+ Triflange | 2025-06-20 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() ULTRA-DRIVE 77816703 not registered Dead/Abandoned |
Overhead Door Corporation 2009-08-31 |
![]() ULTRA-DRIVE 75395686 2293412 Live/Registered |
ROBBINS & MYERS ENERGY SYSTEMS, LP 1997-11-25 |
![]() ULTRA-DRIVE 74306154 not registered Dead/Abandoned |
Whiting Corporation 1992-08-21 |
![]() ULTRA-DRIVE 74214421 1703080 Live/Registered |
Biomet Manufacturing Corp. 1991-10-21 |