MALLORY/HEAD REVISION HIP SYSTEM 104912

GUDID 05019279343232

Biomet Orthopedics, LLC

Coated hip femur prosthesis, modular
Primary Device ID05019279343232
NIH Device Record Keyabc148a4-fd2f-4760-999c-c9927ac7d096
Commercial Distribution StatusIn Commercial Distribution
Brand NameMALLORY/HEAD REVISION HIP SYSTEM
Version Model Number104912
Catalog Number104912
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 Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
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.c

Device Dimensions

Device Size Text, specify0

Device Identifiers

Device Issuing AgencyDevice ID
GS105019279343232 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

MEHProsthesis, hip, semi-constrained, uncemented, metal/polymer, non-porous, calicum-phosphate

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-07-06
Device Publish Date2015-10-24

On-Brand Devices [MALLORY/HEAD REVISION HIP SYSTEM]

00880304441750104917
00880304189942104817
00880304189935104816
00880304189928104815
00880304189904104814
00880304189881104813
00880304189850104811
00880304189836104810
00880304189812104809
00880304005334104812
05019279343263104915
05019279343256104914
05019279343249104913
05019279343232104912
05019279343225104911
05019279343218104910

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