Primary Device ID | 00887868109614 |
NIH Device Record Key | 028dc1e6-f020-49e7-89de-9435ca289811 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | DRILL GUIDE |
Version Model Number | 110008423 |
Catalog Number | 110008423 |
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 | 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 | |
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 | 00887868109614 [Primary] |
HWC | Screw, fixation, bone |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00887868109614]
Moist Heat or Steam Sterilization
[00887868109614]
Moist Heat or Steam Sterilization
[00887868109614]
Moist Heat or Steam Sterilization
[00887868109614]
Moist Heat or Steam Sterilization
[00887868109614]
Moist Heat or Steam Sterilization
[00887868109614]
Moist Heat or Steam Sterilization
[00887868109614]
Moist Heat or Steam Sterilization
[00887868109614]
Moist Heat or Steam Sterilization
[00887868109614]
Moist Heat or Steam Sterilization
[00887868109614]
Moist Heat or Steam Sterilization
[00887868109614]
Moist Heat or Steam Sterilization
[00887868109614]
Moist Heat or Steam Sterilization
[00887868109614]
Moist Heat or Steam Sterilization
[00887868109614]
Moist Heat or Steam Sterilization
[00887868109614]
Moist Heat or Steam Sterilization
[00887868109614]
Moist Heat or Steam Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 5 |
Public Version Date | 2019-08-09 |
Device Publish Date | 2016-09-26 |
00887868109621 | 110008428 |
00887868109607 | 110008418 |
00887868109591 | 110008413 |
00887868073588 | 25-015 |
00887868070709 | DG20 |
00887868024085 | 2141-07-029 |
00887868000621 | 1732 |
00887868109614 | 110008423 |
00887868447266 | 8162-99-012 |
00887868446436 | 8241-64-070 |
00887868446382 | 2141-29-400 |
00887868448652 | DG20 |
00887868463167 | 110008428 |
00887868463150 | 110008423 |
00887868463143 | 110008418 |
00887868463136 | 110008413 |