AGC MODULAR TIBIAL II 32-468414

GUDID 00880304341760

Bone punch, reusable

Primary Device ID	00880304341760
NIH Device Record Key	f7237480-c1d5-41f0-ae96-3aa68674598c
Commercial Distribution Status	In Commercial Distribution
Brand Name	AGC MODULAR TIBIAL II
Version Model Number	32-468414
Catalog Number	32-468414
Company DUNS	129278169
Company Name	Biomet Orthopedics, LLC
Device Count	1
DM Exempt	false
Pre-market Exempt	true
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	true
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)348-9500
Email	customerservice@zimmerbiomet.com

Device Issuing Agency	Device ID
GS1	00880304341760 [Primary]

HWP	PUNCH, FEMORAL NECK

Steralize Prior To Use	true
Device Is Sterile	false

[00880304341760]

Moist Heat or Steam Sterilization