Primary Device ID | 00887868077081 |
NIH Device Record Key | 11d47377-b431-41f1-8554-6dc857887723 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | DVR® CROSSLOCKVOLAR RIM PLATE |
Version Model Number | 131814050 |
Catalog Number | 131814050 |
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 | true |
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 | |
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 Size Text, specify | 0 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00887868077081 [Primary] |
LXT | APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT, METAL COMPOSITE |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00887868077081]
Moist Heat or Steam Sterilization
[00887868077081]
Moist Heat or Steam Sterilization
[00887868077081]
Moist Heat or Steam Sterilization
[00887868077081]
Moist Heat or Steam Sterilization
[00887868077081]
Moist Heat or Steam Sterilization
[00887868077081]
Moist Heat or Steam Sterilization
[00887868077081]
Moist Heat or Steam Sterilization
[00887868077081]
Moist Heat or Steam Sterilization
[00887868077081]
Moist Heat or Steam Sterilization
[00887868077081]
Moist Heat or Steam Sterilization
[00887868077081]
Moist Heat or Steam Sterilization
[00887868077081]
Moist Heat or Steam Sterilization
[00887868077081]
Moist Heat or Steam Sterilization
[00887868077081]
Moist Heat or Steam Sterilization
[00887868077081]
Moist Heat or Steam Sterilization
[00887868077081]
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 | 2016-05-10 |
00880304814806 | 131824051 |
00880304814769 | 131814051 |
00887868077135 | 131825050 |
00887868077128 | 131824050 |
00887868077098 | 131815050 |
00887868077081 | 131814050 |