| Primary Device ID | 00880304676732 |
| NIH Device Record Key | 2eb6412d-0e48-4c11-9a1d-6904190fb4c1 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | VANGUARD TIBIAL BEARING TRIAL ANTERIOR STABILIZED |
| Version Model Number | 32-489061 |
| Catalog Number | 32-489061 |
| 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 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00880304676732 [Primary] |
| JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00880304676732]
Moist Heat or Steam Sterilization
[00880304676732]
Moist Heat or Steam Sterilization
[00880304676732]
Moist Heat or Steam Sterilization
[00880304676732]
Moist Heat or Steam Sterilization
[00880304676732]
Moist Heat or Steam Sterilization
[00880304676732]
Moist Heat or Steam Sterilization
[00880304676732]
Moist Heat or Steam Sterilization
[00880304676732]
Moist Heat or Steam Sterilization
[00880304676732]
Moist Heat or Steam Sterilization
[00880304676732]
Moist Heat or Steam Sterilization
[00880304676732]
Moist Heat or Steam Sterilization
[00880304676732]
Moist Heat or Steam Sterilization
[00880304676732]
Moist Heat or Steam Sterilization
[00880304676732]
Moist Heat or Steam Sterilization
[00880304676732]
Moist Heat or Steam Sterilization
[00880304676732]
Moist Heat or Steam Sterilization
[00880304676732]
Moist Heat or Steam Sterilization
[00880304676732]
Moist Heat or Steam Sterilization
[00880304676732]
Moist Heat or Steam Sterilization
[00880304676732]
Moist Heat or Steam Sterilization
[00880304676732]
Moist Heat or Steam Sterilization
[00880304676732]
Moist Heat or Steam Sterilization
[00880304676732]
Moist Heat or Steam Sterilization
[00880304676732]
Moist Heat or Steam Sterilization
[00880304676732]
Moist Heat or Steam Sterilization
[00880304676732]
Moist Heat or Steam Sterilization
[00880304676732]
Moist Heat or Steam Sterilization
[00880304676732]
Moist Heat or Steam Sterilization
[00880304676732]
Moist Heat or Steam Sterilization
[00880304676732]
Moist Heat or Steam Sterilization
[00880304676732]
Moist Heat or Steam Sterilization
[00880304676732]
Moist Heat or Steam Sterilization
[00880304676732]
Moist Heat or Steam Sterilization
[00880304676732]
Moist Heat or Steam Sterilization
[00880304676732]
Moist Heat or Steam Sterilization
[00880304676732]
Moist Heat or Steam Sterilization
[00880304676732]
Moist Heat or Steam Sterilization
[00880304676732]
Moist Heat or Steam Sterilization
[00880304676732]
Moist Heat or Steam Sterilization
[00880304676732]
Moist Heat or Steam Sterilization
[00880304676732]
Moist Heat or Steam Sterilization
[00880304676732]
Moist Heat or Steam Sterilization
[00880304676732]
Moist Heat or Steam Sterilization
[00880304676732]
Moist Heat or Steam Sterilization
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 6 |
| Public Version Date | 2019-05-30 |
| Device Publish Date | 2016-10-25 |
| 00880304678064 | 32-489003 |
| 00880304678057 | 32-489001 |
| 00880304676763 | 32-489083 |
| 00880304676756 | 32-489081 |
| 00880304676749 | 32-489063 |
| 00880304676732 | 32-489061 |
| 00880304676725 | 32-489043 |
| 00880304676718 | 32-489041 |
| 00880304676701 | 32-489023 |
| 00880304676695 | 32-489021 |
| 00880304613089 | 32-489010 |
| 00880304613072 | 32-489008 |
| 00880304545052 | 32-489006 |
| 00880304545045 | 32-489004 |
| 00880304545038 | 32-489000 |
| 00880304545021 | 32-489002 |