| Primary Device ID | 05019279401765 |
| NIH Device Record Key | 8f73d88a-2e22-4c3e-a6d3-e9b46bbb8049 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | OXFORD UNI KNEE SYSTEM |
| Version Model Number | 32-422835 |
| Catalog Number | 32-422835 |
| Company DUNS | 219322575 |
| Company Name | Biomet Uk Ltd |
| 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)348-9500 |
| customerservice@zimmerbiomet.c |
| Device Size Text, specify | 0 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 05019279401765 [Primary] |
| HWT | TEMPLATE |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[05019279401765]
Moist Heat or Steam Sterilization
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-06-26 |
| Device Publish Date | 2017-07-28 |
| 05019279403776 | 32-422843 |
| 05019279403752 | 32-422842 |
| 05019279401840 | 32-422838 |
| 05019279401826 | 32-422837 |
| 05019279401796 | 32-422836 |
| 05019279401765 | 32-422835 |
| 05019279401604 | 32-422834 |
| 05019279401581 | 32-422833 |
| 05019279401574 | 32-422832 |
| 05019279401550 | 32-422831 |
| 05019279448111 | 32-423242 |
| 05019279448098 | 32-423240 |
| 05019279448067 | 32-423238 |
| 05019279448043 | 32-423236 |
| 05019279448012 | 32-423234 |
| 00880304504714 | 32-422845 |