DRILL GUIDE 110008413

GUDID 00887868109591

Biomet Orthopedics, LLC

Surgical drill guide, reusable
Primary Device ID00887868109591
NIH Device Record Key94b13d87-1f65-4ab7-9e7d-d10b2394baa8
Commercial Distribution StatusIn Commercial Distribution
Brand NameDRILL GUIDE
Version Model Number110008413
Catalog Number110008413
Company DUNS129278169
Company NameBiomet Orthopedics, LLC
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com

Device Dimensions

Device Size Text, specify0

Device Identifiers

Device Issuing AgencyDevice ID
GS100887868109591 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

HWCScrew, fixation, bone

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00887868109591]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2018-11-22
Device Publish Date2016-09-26

On-Brand Devices [DRILL GUIDE]

00887868109621110008428
00887868109607110008418
00887868109591110008413
0088786807358825-015
00887868070709DG20
008878680240852141-07-029
008878680006211732
00887868109614110008423
008878684472668162-99-012
008878684464368241-64-070
008878684463822141-29-400
00887868448652DG20
00887868463167110008428
00887868463150110008423
00887868463143110008418
00887868463136110008413

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