CERAFORM T804415

GUDID 03760177040649

Bone matrix implant, synthetic, non-antimicrobial

Primary Device ID	03760177040649
NIH Device Record Key	20c106ea-f23f-4dac-9be1-dd2e95737a24
Commercial Distribution Status	In Commercial Distribution
Brand Name	CERAFORM
Version Model Number	Granules 3x3x3 30cc
Catalog Number	T804415
Company DUNS	764746723
Company Name	TEKNIMED
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	true
Manufacturing Date	true
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

Device Issuing Agency	Device ID
GS1	03760177040649 [Primary]

MQV	Filler, Bone Void, Calcium Compound

Steralize Prior To Use	false
Device Is Sterile	true

Mark Image Registration \| Serial	Company Trademark Application Date
CERAFORM 87678837 not registered Live/Pending	Northrop Grumman Systems Corporation 2017-11-09
CERAFORM 78970022 not registered Dead/Abandoned	Ceragroup Industries Inc. 2006-09-08
CERAFORM 78218632 not registered Dead/Abandoned	C-MIX CORP. 2003-02-25
CERAFORM 73739649 1525437 Dead/Cancelled	UNITED TECHNOLOGIES OPTICAL SYSTEMS, INC. 1988-07-13
CERAFORM 73739644 1525436 Dead/Cancelled	UNITED TECHNOLOGIES OPTICAL SYSTEMS, INC. 1988-07-13
CERAFORM 73454145 1384997 Dead/Cancelled	Kollmorgen Corporation 1983-11-23