Primary Device ID | 00880304516137 |
NIH Device Record Key | 533a0a66-204f-44ec-84e6-57507160fba2 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | VANGUARD |
Version Model Number | 32-360508 |
Catalog Number | 32-360508 |
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 |
Phone | +1(800)348-9500 |
customerservice@zimmerbiomet.com | |
Phone | +1(800)348-9500 |
customerservice@zimmerbiomet.com | |
Phone | +1(800)348-9500 |
customerservice@zimmerbiomet.com | |
Phone | +1(800)348-9500 |
customerservice@zimmerbiomet.com | |
Phone | +1(800)348-9500 |
customerservice@zimmerbiomet.com | |
Phone | +1(800)348-9500 |
customerservice@zimmerbiomet.com | |
Phone | +1(800)348-9500 |
customerservice@zimmerbiomet.com | |
Phone | +1(800)348-9500 |
customerservice@zimmerbiomet.com | |
Phone | +1(800)348-9500 |
customerservice@zimmerbiomet.com | |
Phone | +1(800)348-9500 |
customerservice@zimmerbiomet.com | |
Phone | +1(800)348-9500 |
customerservice@zimmerbiomet.com | |
Phone | +1(800)348-9500 |
customerservice@zimmerbiomet.com | |
Phone | +1(800)348-9500 |
customerservice@zimmerbiomet.com | |
Phone | +1(800)348-9500 |
customerservice@zimmerbiomet.com |
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 | 00880304516137 [Primary] |
MBV | Prosthesis, knee, patello/femorotibial, semi-constrained, uhmwpe, pegged, cemented, polymer/metal/polymer |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00880304516137]
Moist Heat or Steam Sterilization
[00880304516137]
Moist Heat or Steam Sterilization
[00880304516137]
Moist Heat or Steam Sterilization
[00880304516137]
Moist Heat or Steam Sterilization
[00880304516137]
Moist Heat or Steam Sterilization
[00880304516137]
Moist Heat or Steam Sterilization
[00880304516137]
Moist Heat or Steam Sterilization
[00880304516137]
Moist Heat or Steam Sterilization
[00880304516137]
Moist Heat or Steam Sterilization
[00880304516137]
Moist Heat or Steam Sterilization
[00880304516137]
Moist Heat or Steam Sterilization
[00880304516137]
Moist Heat or Steam Sterilization
[00880304516137]
Moist Heat or Steam Sterilization
[00880304516137]
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 | 2016-09-21 |