Primary Device ID | 00887868484629 |
NIH Device Record Key | 50ae7cad-ad9e-4704-bd4e-13ae56d3c086 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Vanguard® 360 Instrument |
Version Model Number | 32-360828 |
Catalog Number | 32-360828 |
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 | 00887868484629 [Primary] |
MBH | PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SEMI-CONSTRAINED, UNCEMENTED, POROUS, COATED, POLYMER/METAL/POLYMER |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00887868484629]
Moist Heat or Steam Sterilization
[00887868484629]
Moist Heat or Steam Sterilization
[00887868484629]
Moist Heat or Steam Sterilization
[00887868484629]
Moist Heat or Steam Sterilization
[00887868484629]
Moist Heat or Steam Sterilization
[00887868484629]
Moist Heat or Steam Sterilization
[00887868484629]
Moist Heat or Steam Sterilization
[00887868484629]
Moist Heat or Steam Sterilization
[00887868484629]
Moist Heat or Steam Sterilization
[00887868484629]
Moist Heat or Steam Sterilization
[00887868484629]
Moist Heat or Steam Sterilization
[00887868484629]
Moist Heat or Steam Sterilization
[00887868484629]
Moist Heat or Steam Sterilization
[00887868484629]
Moist Heat or Steam Sterilization
[00887868484629]
Moist Heat or Steam Sterilization
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-04-11 |
Device Publish Date | 2022-04-02 |