Primary Device ID | 00888480153214 |
NIH Device Record Key | dfd77150-d983-4918-ae64-ef4418de5c23 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | XS MULTI-AXIAL CORRECTION SYSTEM |
Version Model Number | 13110 |
Catalog Number | 13110 |
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 | |
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 Size Text, specify | 0 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00888480153214 [Primary] |
KTT | APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00888480153214]
Moist Heat or Steam Sterilization
[00888480153214]
Moist Heat or Steam Sterilization
[00888480153214]
Moist Heat or Steam Sterilization
[00888480153214]
Moist Heat or Steam Sterilization
[00888480153214]
Moist Heat or Steam Sterilization
[00888480153214]
Moist Heat or Steam Sterilization
[00888480153214]
Moist Heat or Steam Sterilization
[00888480153214]
Moist Heat or Steam Sterilization
[00888480153214]
Moist Heat or Steam Sterilization
[00888480153214]
Moist Heat or Steam Sterilization
[00888480153214]
Moist Heat or Steam Sterilization
[00888480153214]
Moist Heat or Steam Sterilization
[00888480153214]
Moist Heat or Steam Sterilization
[00888480153214]
Moist Heat or Steam Sterilization
[00888480153214]
Moist Heat or Steam Sterilization
[00888480153214]
Moist Heat or Steam Sterilization
[00888480153214]
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 |
00880304534650 | 15265 |
00880304533776 | 15280 |
00880304533769 | 15244 |
00880304532427 | 15285 |
00888480190509 | 15295 |
00888480190448 | 15275 |
00888480190349 | 15245 |
00888480190318 | 15230 |
00888480153221 | 13115 |
00888480153214 | 13110 |
00888480153207 | 13105 |
00880304591905 | 14-415360 |