Primary Device ID | 00880304533363 |
NIH Device Record Key | 7eb6b13f-0494-45b2-a5e7-524c1be526ee |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | DVR® CROSSLOCKNARROW MINI PLATE RIGHT (HEAD WIDTH X OVERALL LENGTH) |
Version Model Number | 1318-11-040 |
Catalog Number | 131811040 |
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 | 00880304533363 [Primary] |
LXT | APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT, METAL COMPOSITE |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00880304533363]
Moist Heat or Steam Sterilization
[00880304533363]
Moist Heat or Steam Sterilization
[00880304533363]
Moist Heat or Steam Sterilization
[00880304533363]
Moist Heat or Steam Sterilization
[00880304533363]
Moist Heat or Steam Sterilization
[00880304533363]
Moist Heat or Steam Sterilization
[00880304533363]
Moist Heat or Steam Sterilization
[00880304533363]
Moist Heat or Steam Sterilization
[00880304533363]
Moist Heat or Steam Sterilization
[00880304533363]
Moist Heat or Steam Sterilization
[00880304533363]
Moist Heat or Steam Sterilization
[00880304533363]
Moist Heat or Steam Sterilization
[00880304533363]
Moist Heat or Steam Sterilization
[00880304533363]
Moist Heat or Steam Sterilization
[00880304533363]
Moist Heat or Steam Sterilization
[00880304533363]
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 |
00880304811829 | 1318-11-041 |
00880304533363 | 1318-11-040 |