| Primary Device ID | 00810041063458 |
| NIH Device Record Key | 4fb38c60-9e6b-43fe-8531-67ba7e6e38b4 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Biomet |
| Version Model Number | 506113 |
| Company DUNS | 016889401 |
| Company Name | Provision |
| Device Count | 1 |
| DM Exempt | true |
| 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 | true |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | true |
| 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 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00810041063458 [Primary] |
| GFA | Blade, Saw, General & Plastic Surgery, Surgical |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2020-04-30 |
| Device Publish Date | 2019-12-11 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() BIOMET 79083976 not registered Dead/Abandoned |
VEOLIA WATER TECHNOLOGIES ITALIA S.p.A. 2010-03-23 |
![]() BIOMET 78703978 3176481 Live/Registered |
ZIMMER, INC. 2005-08-31 |
![]() BIOMET 78498921 3235830 Dead/Cancelled |
ARKEMA, INC. 2004-10-13 |
![]() BIOMET 75282520 2301253 Live/Registered |
ZIMMER, INC. 1997-04-10 |
![]() BIOMET 74722414 not registered Dead/Abandoned |
NOREL, S.A. 1995-08-29 |
![]() BIOMET 73585352 1411822 Live/Registered |
BIOMET, INC. 1986-02-28 |
![]() BIOMET 73165517 1153792 Live/Registered |
BIOMET, INC. 1978-04-07 |