Primary Device ID | 00880304443617 |
NIH Device Record Key | 88f5da74-e262-48d6-9867-b04386502d72 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | VANGUARD UNIVERSAL 5-IN-1 TIBIAL |
Version Model Number | 32-483812 |
Catalog Number | 32-483812 |
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 | false |
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 Issuing Agency | Device ID |
---|---|
GS1 | 00880304443617 [Primary] |
OIY | Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer + additive/metal/polymer + additive |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00880304443617]
Moist Heat or Steam Sterilization
[00880304443617]
Moist Heat or Steam Sterilization
[00880304443617]
Moist Heat or Steam Sterilization
[00880304443617]
Moist Heat or Steam Sterilization
[00880304443617]
Moist Heat or Steam Sterilization
[00880304443617]
Moist Heat or Steam Sterilization
[00880304443617]
Moist Heat or Steam Sterilization
[00880304443617]
Moist Heat or Steam Sterilization
[00880304443617]
Moist Heat or Steam Sterilization
[00880304443617]
Moist Heat or Steam Sterilization
[00880304443617]
Moist Heat or Steam Sterilization
[00880304443617]
Moist Heat or Steam Sterilization
[00880304443617]
Moist Heat or Steam Sterilization
[00880304443617]
Moist Heat or Steam Sterilization
[00880304443617]
Moist Heat or Steam Sterilization
[00880304443617]
Moist Heat or Steam Sterilization
[00880304443617]
Moist Heat or Steam Sterilization
[00880304443617]
Moist Heat or Steam Sterilization
[00880304443617]
Moist Heat or Steam Sterilization
[00880304443617]
Moist Heat or Steam Sterilization
[00880304443617]
Moist Heat or Steam Sterilization
[00880304443617]
Moist Heat or Steam Sterilization
[00880304443617]
Moist Heat or Steam Sterilization
[00880304443617]
Moist Heat or Steam Sterilization
[00880304443617]
Moist Heat or Steam Sterilization
[00880304443617]
Moist Heat or Steam Sterilization
[00880304443617]
Moist Heat or Steam Sterilization
[00880304443617]
Moist Heat or Steam Sterilization
[00880304443617]
Moist Heat or Steam Sterilization
[00880304443617]
Moist Heat or Steam Sterilization
[00880304443617]
Moist Heat or Steam Sterilization
[00880304443617]
Moist Heat or Steam Sterilization
[00880304443617]
Moist Heat or Steam Sterilization
[00880304443617]
Moist Heat or Steam Sterilization
[00880304443617]
Moist Heat or Steam Sterilization
[00880304443617]
Moist Heat or Steam Sterilization
[00880304443617]
Moist Heat or Steam Sterilization
[00880304443617]
Moist Heat or Steam Sterilization
[00880304443617]
Moist Heat or Steam Sterilization
[00880304443617]
Moist Heat or Steam Sterilization
[00880304443617]
Moist Heat or Steam Sterilization
[00880304443617]
Moist Heat or Steam Sterilization
[00880304443617]
Moist Heat or Steam Sterilization
[00880304443617]
Moist Heat or Steam Sterilization
[00880304443617]
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 | 2016-09-22 |
00880304443877 | 32-483830 |
00880304443860 | 32-483824 |
00880304443853 | 32-483820 |
00880304443846 | 32-483822 |
00880304443839 | 32-483828 |
00880304443822 | 32-483848 |
00880304443815 | 32-483864 |
00880304443808 | 32-483842 |
00880304443792 | 32-483826 |
00880304443785 | 32-483850 |
00880304443778 | 32-483844 |
00880304443761 | 32-483846 |
00880304443730 | 32-483840 |
00880304443716 | 32-483832 |
00880304443709 | 32-483860 |
00880304443693 | 32-483834 |
00880304443679 | 32-483852 |
00880304443655 | 32-483814 |
00880304443631 | 32-483854 |
00880304443624 | 32-483862 |
00880304443617 | 32-483812 |
00880304436596 | 32-483800 |
00880304436589 | 32-483808 |
00880304436572 | 32-483806 |
00880304436558 | 32-483804 |
00880304436534 | 32-483802 |
00880304436510 | 32-483810 |