MALLORY/HEAD REVISION HIP SYSTEM 104912

GUDID 05019279343232

Coated hip femur prosthesis, modular

Primary Device ID	05019279343232
NIH Device Record Key	abc148a4-fd2f-4760-999c-c9927ac7d096
Commercial Distribution Status	In Commercial Distribution
Brand Name	MALLORY/HEAD REVISION HIP SYSTEM
Version Model Number	104912
Catalog Number	104912
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	true
Lot Batch	true
Serial Number	false
Manufacturing Date	false
Expiration Date	true
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
Email	customerservice@zimmerbiomet.c

Device Size Text, specify

Device Issuing Agency	Device ID
GS1	05019279343232 [Primary]

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

Steralize Prior To Use	false
Device Is Sterile	true