Primary Device ID | 00887868044830 |
NIH Device Record Key | fc44283c-8dc1-4477-92e8-09a407450100 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | LOCKING COMPRESSION PLATE |
Version Model Number | 8162-35-008 |
Catalog Number | 816235008 |
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 | 00887868044830 [Primary] |
LXT | APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT, METAL COMPOSITE |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00887868044830]
Moist Heat or Steam Sterilization
[00887868044830]
Moist Heat or Steam Sterilization
[00887868044830]
Moist Heat or Steam Sterilization
[00887868044830]
Moist Heat or Steam Sterilization
[00887868044830]
Moist Heat or Steam Sterilization
[00887868044830]
Moist Heat or Steam Sterilization
[00887868044830]
Moist Heat or Steam Sterilization
[00887868044830]
Moist Heat or Steam Sterilization
[00887868044830]
Moist Heat or Steam Sterilization
[00887868044830]
Moist Heat or Steam Sterilization
[00887868044830]
Moist Heat or Steam Sterilization
[00887868044830]
Moist Heat or Steam Sterilization
[00887868044830]
Moist Heat or Steam Sterilization
[00887868044830]
Moist Heat or Steam Sterilization
[00887868044830]
Moist Heat or Steam Sterilization
[00887868044830]
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 | 2015-10-24 |
00887868044878 | 8162-35-014 |
00887868044861 | 8162-35-012 |
00887868044854 | 8162-35-010 |
00887868044847 | 8162-35-009 |
00887868044830 | 8162-35-008 |
00887868044823 | 8162-35-007 |
00887868044816 | 8162-35-006 |
00887868044809 | 8162-35-005 |