COMPREHENSIVE INSTRUMENTS 010001787

GUDID 00880304564367

Biomet Orthopedics, LLC

Glenoid orthopaedic reamer
Primary Device ID00880304564367
NIH Device Record Key288d8d42-17bd-4261-9d3c-d330eb282923
Commercial Distribution StatusIn Commercial Distribution
Brand NameCOMPREHENSIVE INSTRUMENTS
Version Model Number010001787
Catalog Number010001787
Company DUNS129278169
Company NameBiomet Orthopedics, LLC
Device Count1
DM Exemptfalse
Pre-market Exempttrue
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 Datetrue
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 Identifiers

Device Issuing AgencyDevice ID
GS100880304564367 [Primary]

FDA Product Code

HTOREAMER

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00880304564367]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2019-04-26
Device Publish Date2019-04-18

On-Brand Devices [COMPREHENSIVE INSTRUMENTS]

00880304539433110003472
00880304539426110003483
00880304539419110003478
00880304539402110003476
00880304539396110003474
00880304539389110004265
00880304539372010001791
00880304539365010001800
00880304539358010001801
00880304539341010001799
00880304539334010001790
00880304539327010001792
00880304539310110004200
00880304539303110003486
00880304539280110003488
00880304537781110003484
00880304537026110003489
00880304564381010001789
00880304564374010001788
00880304564367010001787

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