Primary Device ID | 00887868446504 |
NIH Device Record Key | 500dd787-178a-4982-9c7b-8a1b3cd34caa |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | LOCKING DRILL GUIDE |
Version Model Number | 2142-07-027 |
Catalog Number | 214207027 |
Company DUNS | 129278169 |
Company Name | Biomet Orthopedics, LLC |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | false |
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 |
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 | 00887868446504 [Primary] |
FZX | Guide, surgical, instrument |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00887868446504]
Moist Heat or Steam Sterilization
[00887868446504]
Moist Heat or Steam Sterilization
[00887868446504]
Moist Heat or Steam Sterilization
[00887868446504]
Moist Heat or Steam Sterilization
[00887868446504]
Moist Heat or Steam Sterilization
[00887868446504]
Moist Heat or Steam Sterilization
[00887868446504]
Moist Heat or Steam Sterilization
[00887868446504]
Moist Heat or Steam Sterilization
[00887868446504]
Moist Heat or Steam Sterilization
[00887868446504]
Moist Heat or Steam Sterilization
[00887868446504]
Moist Heat or Steam Sterilization
[00887868446504]
Moist Heat or Steam Sterilization
[00887868446504]
Moist Heat or Steam Sterilization
[00887868446504]
Moist Heat or Steam Sterilization
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2020-09-14 |
Device Publish Date | 2020-09-04 |
00880304533554 | 2312-00-109 |
00887868446504 | 2142-07-027 |
00887868445736 | 2142-07-020 |