DuraMatrix

GUDID 00813954020204

Dura mater biomatrix implant

Primary Device ID	00813954020204
NIH Device Record Key	abf69533-bc2a-4dc9-a9d9-2d6fa0a8927c
Commercial Distribution Status	In Commercial Distribution
Brand Name	DuraMatrix
Version Model Number	CDSM22
Company DUNS	176262442
Company Name	COLLAGEN MATRIX, 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	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

Device Issuing Agency	Device ID
GS1	00813954020204 [Primary]

GXQ	Dura Substitute

Steralize Prior To Use	false
Device Is Sterile	true

00813954020228	Collagen Dura Substitute Membrane 4in x 5in (10.0cm x 12.5cm)
00813954020211	Collagen Dura Substitute Membrane 3in x 3in (7.5cm x 7.5cm)
00813954020204	Collagen Dura Substitute Membrane 2in x 2in (5cm x 5cm)
00813954020198	Collagen Dura Substitute Membrane 1in x 3in (2.5cm x 7.5cm)
00813954020181	Collagen Dura Substitute Membrane 1in x 1in (2.5cm x 2.5cm)

Mark Image Registration \| Serial	Company Trademark Application Date
DURAMATRIX 85657920 4327230 Live/Registered	Collagen Matrix, Inc. 2012-06-21
DURAMATRIX 85243608 4022800 Dead/Cancelled	Duragraft, LLC 2011-02-16