| Primary Device ID | 00880304676794 | 
| NIH Device Record Key | 8b82da5d-3dc4-4ac5-80e3-b9e79f0bcb3f | 
| Commercial Distribution Status | In Commercial Distribution | 
| Brand Name | VANGUARD® TIBIAL TRIAL BEARING | 
| Version Model Number | 32-489121 | 
| Catalog Number | 32-489121 | 
| 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 | 00880304676794 [Primary] | 
| JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 
| Steralize Prior To Use | true | 
| Device Is Sterile | false | 
[00880304676794]
Moist Heat or Steam Sterilization
[00880304676794]
Moist Heat or Steam Sterilization
[00880304676794]
Moist Heat or Steam Sterilization
[00880304676794]
Moist Heat or Steam Sterilization
[00880304676794]
Moist Heat or Steam Sterilization
[00880304676794]
Moist Heat or Steam Sterilization
[00880304676794]
Moist Heat or Steam Sterilization
[00880304676794]
Moist Heat or Steam Sterilization
[00880304676794]
Moist Heat or Steam Sterilization
[00880304676794]
Moist Heat or Steam Sterilization
[00880304676794]
Moist Heat or Steam Sterilization
[00880304676794]
Moist Heat or Steam Sterilization
[00880304676794]
Moist Heat or Steam Sterilization
[00880304676794]
Moist Heat or Steam Sterilization
[00880304676794]
Moist Heat or Steam Sterilization
[00880304676794]
Moist Heat or Steam Sterilization
[00880304676794]
Moist Heat or Steam Sterilization
[00880304676794]
Moist Heat or Steam Sterilization
[00880304676794]
Moist Heat or Steam Sterilization
[00880304676794]
Moist Heat or Steam Sterilization
[00880304676794]
Moist Heat or Steam Sterilization
[00880304676794]
Moist Heat or Steam Sterilization
[00880304676794]
Moist Heat or Steam Sterilization
[00880304676794]
Moist Heat or Steam Sterilization
[00880304676794]
Moist Heat or Steam Sterilization
[00880304676794]
Moist Heat or Steam Sterilization
[00880304676794]
Moist Heat or Steam Sterilization
[00880304676794]
Moist Heat or Steam Sterilization
[00880304676794]
Moist Heat or Steam Sterilization
[00880304676794]
Moist Heat or Steam Sterilization
[00880304676794]
Moist Heat or Steam Sterilization
[00880304676794]
Moist Heat or Steam Sterilization
[00880304676794]
Moist Heat or Steam Sterilization
[00880304676794]
Moist Heat or Steam Sterilization
[00880304676794]
Moist Heat or Steam Sterilization
[00880304676794]
Moist Heat or Steam Sterilization
[00880304676794]
Moist Heat or Steam Sterilization
[00880304676794]
Moist Heat or Steam Sterilization
[00880304676794]
Moist Heat or Steam Sterilization
[00880304676794]
Moist Heat or Steam Sterilization
[00880304676794]
Moist Heat or Steam Sterilization
[00880304676794]
Moist Heat or Steam Sterilization
[00880304676794]
Moist Heat or Steam Sterilization
[00880304676794]
Moist Heat or Steam Sterilization
| Public Version Status | Update | 
| Device Record Status | Published | 
| Public Version Number | 5 | 
| Public Version Date | 2019-02-07 | 
| Device Publish Date | 2016-10-25 | 
| 00880304676800 | 32-489123 | 
| 00880304676794 | 32-489121 | 
| 00880304676787 | 32-489103 | 
| 00880304676770 | 32-489101 |