OptiMatrix™ Extracellular Matrix 40-2030

GUDID 00812337027083

DSM BIOMEDICAL, INC.

Collagen dental regeneration membrane Collagen dental regeneration membrane Collagen dental regeneration membrane Collagen dental regeneration membrane Collagen dental regeneration membrane Collagen dental regeneration membrane Collagen dental regeneration membrane Collagen dental regeneration membrane Collagen dental regeneration membrane Collagen dental regeneration membrane Collagen dental regeneration membrane Collagen dental regeneration membrane Collagen dental regeneration membrane Collagen dental regeneration membrane Collagen dental regeneration membrane Collagen dental regeneration membrane Collagen dental regeneration membrane Collagen dental regeneration membrane

Primary Device ID	00812337027083
NIH Device Record Key	cd3858b5-aa6e-4ade-b32d-b487d8a4b8b9
Commercial Distribution Discontinuation	2019-09-30
Commercial Distribution Status	Not in Commercial Distribution
Brand Name	OptiMatrix™ Extracellular Matrix
Version Model Number	30053-02
Catalog Number	40-2030
Company DUNS	131107757
Company Name	DSM BIOMEDICAL, 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 Dimensions

Width	20 Millimeter
Width	20 Millimeter
Width	20 Millimeter
Width	20 Millimeter
Length	30 Millimeter
Width	20 Millimeter
Length	30 Millimeter
Width	20 Millimeter
Length	30 Millimeter
Width	20 Millimeter
Length	30 Millimeter
Width	20 Millimeter
Length	30 Millimeter
Width	20 Millimeter
Length	30 Millimeter
Width	20 Millimeter
Length	30 Millimeter
Width	20 Millimeter
Length	30 Millimeter
Width	20 Millimeter
Length	30 Millimeter
Width	20 Millimeter
Length	30 Millimeter
Width	20 Millimeter
Length	30 Millimeter
Width	20 Millimeter
Length	30 Millimeter
Width	20 Millimeter
Length	30 Millimeter
Width	20 Millimeter
Length	30 Millimeter
Width	20 Millimeter
Length	30 Millimeter
Width	20 Millimeter
Length	30 Millimeter
Width	20 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	00812337027083 [Primary]

FDA Product Code

NPL	Barrier, Animal Source, Intraoral

Sterilization

Steralize Prior To Use	false
Device Is Sterile	true

Device Entry Metadata

Public Version Status	Update
Device Record Status	Published
Public Version Number	4
Public Version Date	2019-10-01
Device Publish Date	2015-09-17

On-Brand Devices [OptiMatrix™ Extracellular Matrix ]

00812337027090	30053-03
00812337027083	30053-02
00812337027076	30053-01

Trademark Results [OptiMatrix]

Mark Image Registration \| Serial	Company Trademark Application Date
OPTIMATRIX 85581807 4548136 Live/Registered	AMERICAN REGENT, INC. 2012-03-28
OPTIMATRIX 74691119 2058652 Dead/Cancelled	OPTIMATRIX HEALTH SOLUTIONS, INC. 1995-06-19
OPTIMATRIX 73731610 1542914 Dead/Cancelled	SAFF, ROBERT E. 1988-05-31
OPTIMATRIX 73673076 not registered Dead/Abandoned	R. E. SAFF-MANAGEMENT ANALYST 1987-07-20