COMPREHENSIVE INSTRUMENTATION 405960

GUDID 00880304470279

Biomet Orthopedics, LLC

Humeral head prosthesis trial, reusable
Primary Device ID00880304470279
NIH Device Record Keya63a00bd-8bbe-4dfb-b044-ee78f349025f
Commercial Distribution StatusIn Commercial Distribution
Brand NameCOMPREHENSIVE INSTRUMENTATION
Version Model Number405960
Catalog Number405960
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
GS100880304470279 [Primary]

FDA Product Code

HWTTEMPLATE

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00880304470279]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2019-05-30
Device Publish Date2017-07-28

On-Brand Devices [COMPREHENSIVE INSTRUMENTATION]

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00880304469716405802

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