Primary Device ID | 00880304448100 |
NIH Device Record Key | 842837f3-7544-450b-812e-1979d1890325 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | VANGUARD(TM) REVISION TRIAL PLATE |
Version Model Number | 32-488268 |
Catalog Number | 32-488268 |
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 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 | 00880304448100 [Primary] |
MBH | PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SEMI-CONSTRAINED, UNCEMENTED, POROUS, COATED, POLYMER/METAL/POLYMER |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00880304448100]
Moist Heat or Steam Sterilization
[00880304448100]
Moist Heat or Steam Sterilization
[00880304448100]
Moist Heat or Steam Sterilization
[00880304448100]
Moist Heat or Steam Sterilization
[00880304448100]
Moist Heat or Steam Sterilization
[00880304448100]
Moist Heat or Steam Sterilization
[00880304448100]
Moist Heat or Steam Sterilization
[00880304448100]
Moist Heat or Steam Sterilization
[00880304448100]
Moist Heat or Steam Sterilization
[00880304448100]
Moist Heat or Steam Sterilization
[00880304448100]
Moist Heat or Steam Sterilization
[00880304448100]
Moist Heat or Steam Sterilization
[00880304448100]
Moist Heat or Steam Sterilization
[00880304448100]
Moist Heat or Steam Sterilization
[00880304448100]
Moist Heat or Steam Sterilization
[00880304448100]
Moist Heat or Steam Sterilization
[00880304448100]
Moist Heat or Steam Sterilization
[00880304448100]
Moist Heat or Steam Sterilization
[00880304448100]
Moist Heat or Steam Sterilization
[00880304448100]
Moist Heat or Steam Sterilization
[00880304448100]
Moist Heat or Steam Sterilization
[00880304448100]
Moist Heat or Steam Sterilization
[00880304448100]
Moist Heat or Steam Sterilization
[00880304448100]
Moist Heat or Steam Sterilization
[00880304448100]
Moist Heat or Steam Sterilization
[00880304448100]
Moist Heat or Steam Sterilization
[00880304448100]
Moist Heat or Steam Sterilization
[00880304448100]
Moist Heat or Steam Sterilization
[00880304448100]
Moist Heat or Steam Sterilization
[00880304448100]
Moist Heat or Steam Sterilization
[00880304448100]
Moist Heat or Steam Sterilization
[00880304448100]
Moist Heat or Steam Sterilization
[00880304448100]
Moist Heat or Steam Sterilization
[00880304448100]
Moist Heat or Steam Sterilization
[00880304448100]
Moist Heat or Steam Sterilization
[00880304448100]
Moist Heat or Steam Sterilization
[00880304448100]
Moist Heat or Steam Sterilization
[00880304448100]
Moist Heat or Steam Sterilization
[00880304448100]
Moist Heat or Steam Sterilization
[00880304448100]
Moist Heat or Steam Sterilization
[00880304448100]
Moist Heat or Steam Sterilization
[00880304448100]
Moist Heat or Steam Sterilization
[00880304448100]
Moist Heat or Steam Sterilization
[00880304448100]
Moist Heat or Steam Sterilization
[00880304448100]
Moist Heat or Steam Sterilization
[00880304448100]
Moist Heat or Steam Sterilization
[00880304448100]
Moist Heat or Steam Sterilization
[00880304448100]
Moist Heat or Steam Sterilization
[00880304448100]
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 | 2016-10-26 |
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08428898885684 - BIPASS DISPOSABLE PUSHER | 2024-09-11 |
08428898885691 - BIPASS DISPOSABLE PUSHER | 2024-09-11 |
00880304338548 - AGC ANTERIOR FILE | 2024-09-11 |
00880304339224 - PARALLEL PULLER | 2024-09-11 |
00880304342187 - AGC MODULAR TIBIAL II | 2024-09-11 |
00880304365247 - BIO-MODULAR | 2024-09-11 |