802503204

GUDID 00889024499478

Femoral head prosthesis trial

Primary Device ID	00889024499478
NIH Device Record Key	2faf5b8b-7659-4e06-97c6-69a1a0567c77
Commercial Distribution Status	In Commercial Distribution
Version Model Number	802503204
Catalog Number	802503204
Company DUNS	056038268
Company Name	Zimmer, Inc.
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	false
Lot Batch	false
Serial Number	false
Manufacturing Date	false
Expiration Date	false
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)348-2759
Email	zimmer.consumerrelations@zimmerbiomet.com

Device Size Text, specify

Device Issuing Agency	Device ID
GS1	00889024499478 [Primary]

LPH	PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED

Steralize Prior To Use	true
Device Is Sterile	false

[00889024499478]

Moist Heat or Steam Sterilization