Primary Device ID | 00887868004001 |
NIH Device Record Key | a56fdb79-e01c-48da-b097-fbb6cb7fc446 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | GUIDE WIRE |
Version Model Number | 14012-9 |
Catalog Number | 140129 |
Company DUNS | 129278169 |
Company Name | Biomet Orthopedics, LLC |
Device Count | 3 |
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 | 00887868004001 [Primary] |
GS1 | 70887868004000 [Unit of Use] |
KTT | APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00887868004001]
Moist Heat or Steam Sterilization
[00887868004001]
Moist Heat or Steam Sterilization
[00887868004001]
Moist Heat or Steam Sterilization
[00887868004001]
Moist Heat or Steam Sterilization
[00887868004001]
Moist Heat or Steam Sterilization
[00887868004001]
Moist Heat or Steam Sterilization
[00887868004001]
Moist Heat or Steam Sterilization
[00887868004001]
Moist Heat or Steam Sterilization
[00887868004001]
Moist Heat or Steam Sterilization
[00887868004001]
Moist Heat or Steam Sterilization
[00887868004001]
Moist Heat or Steam Sterilization
[00887868004001]
Moist Heat or Steam Sterilization
[00887868004001]
Moist Heat or Steam Sterilization
[00887868004001]
Moist Heat or Steam Sterilization
[00887868004001]
Moist Heat or Steam Sterilization
[00887868004001]
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 |
00887868005251 | 1724-28 |
00887868004001 | 14012-9 |
00887868510700 | 8092-22-028 |
70887868004000 | 14012-9 |
00880304415959 | 945020 |
00887868556876 | 909894 |
00887868034701 | 8092-32-238 |
00887868034695 | 8092-32-228 |
00887868034664 | 8092-22-028 |
00887868003936 | 1075-38 |
00887868003929 | 1075-28 |