OSSEOTI RECONSTRUCTIVE SYSTEM 110003772

GUDID 00887868130922

Bone matrix implant, synthetic

Primary Device ID	00887868130922
NIH Device Record Key	8dc45ea8-98da-44cd-b642-c166c570cf2a
Commercial Distribution Status	In Commercial Distribution
Brand Name	OSSEOTI RECONSTRUCTIVE SYSTEM
Version Model Number	110003772
Catalog Number	110003772
Company DUNS	129278169
Company Name	Biomet Orthopedics, LLC
Device Count	1
DM Exempt	false
Pre-market Exempt	false
MRI Safety Status	MR Conditional
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.com

Device Size Text, specify

Device Issuing Agency	Device ID
GS1	00887868130922 [Primary]

HWC	Screw, fixation, bone

Steralize Prior To Use	false
Device Is Sterile	true