Primary Device ID | 00887868484667 |
NIH Device Record Key | 932bc0d3-7486-4a3e-8ffc-5149476f1461 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Vanguard® 360 Instrument |
Version Model Number | 32-360882 |
Catalog Number | 32-360882 |
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 | |
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 Size Text, specify | 0 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00887868484667 [Primary] |
JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00887868484667]
Moist Heat or Steam Sterilization
[00887868484667]
Moist Heat or Steam Sterilization
[00887868484667]
Moist Heat or Steam Sterilization
[00887868484667]
Moist Heat or Steam Sterilization
[00887868484667]
Moist Heat or Steam Sterilization
[00887868484667]
Moist Heat or Steam Sterilization
[00887868484667]
Moist Heat or Steam Sterilization
[00887868484667]
Moist Heat or Steam Sterilization
[00887868484667]
Moist Heat or Steam Sterilization
[00887868484667]
Moist Heat or Steam Sterilization
[00887868484667]
Moist Heat or Steam Sterilization
[00887868484667]
Moist Heat or Steam Sterilization
[00887868484667]
Moist Heat or Steam Sterilization
[00887868484667]
Moist Heat or Steam Sterilization
[00887868484667]
Moist Heat or Steam Sterilization
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2021-05-10 |
Device Publish Date | 2021-04-30 |