| Primary Device ID | 00880304543539 |
| NIH Device Record Key | 19f5c551-66f3-4545-b757-72100d92a124 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | OXFORD LATERAL INSTRUMENTS |
| Version Model Number | 32-423343 |
| Catalog Number | 32-423343 |
| 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 | false |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | true |
| 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.com |
| Device Size Text, specify | 0 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00880304543539 [Primary] |
| HRY | PROSTHESIS, KNEE, FEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00880304543539]
Moist Heat or Steam Sterilization
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2016-10-21 |
| 00880304609952 | 32-423353 |
| 00880304609945 | 32-423350 |
| 00880304609884 | 32-423339 |
| 00880304543560 | 32-423352 |
| 00880304543553 | 32-423351 |
| 00880304543546 | 32-423341 |
| 00880304543539 | 32-423343 |
| 00880304543522 | 32-423344 |
| 00880304543478 | 32-423342 |
| 00880304543447 | 32-423340 |
| 00880304543430 | 32-423337 |
| 00880304543423 | 32-423338 |