OptiMatrix™ Extracellular Matrix 40-3040
GUDID 00812337027090
DSM BIOMEDICAL, INC.
Collagen dental regeneration membrane| Primary Device ID | 00812337027090 |
| NIH Device Record Key | 765ac8d4-2c09-419f-b65f-aba0bc4d06e3 |
| Commercial Distribution Discontinuation | 2019-09-30 |
| Commercial Distribution Status | Not in Commercial Distribution |
| Brand Name | OptiMatrix™ Extracellular Matrix |
| Version Model Number | 30053-03 |
| Catalog Number | 40-3040 |
| 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 | 30 Millimeter |
| Width | 30 Millimeter |
| Width | 30 Millimeter |
| Width | 30 Millimeter |
| Length | 40 Millimeter |
| Width | 30 Millimeter |
| Length | 40 Millimeter |
| Width | 30 Millimeter |
| Length | 40 Millimeter |
| Width | 30 Millimeter |
| Length | 40 Millimeter |
| Width | 30 Millimeter |
| Length | 40 Millimeter |
| Width | 30 Millimeter |
| Length | 40 Millimeter |
| Width | 30 Millimeter |
| Length | 40 Millimeter |
| Width | 30 Millimeter |
| Length | 40 Millimeter |
| Width | 30 Millimeter |
| Length | 40 Millimeter |
| Width | 30 Millimeter |
| Length | 40 Millimeter |
| Width | 30 Millimeter |
| Length | 40 Millimeter |
| Width | 30 Millimeter |
| Length | 40 Millimeter |
| Width | 30 Millimeter |
| Length | 40 Millimeter |
| Width | 30 Millimeter |
| Length | 40 Millimeter |
| Width | 30 Millimeter |
| Length | 40 Millimeter |
| Width | 30 Millimeter |
| Length | 40 Millimeter |
| Width | 30 Millimeter |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00812337027090 [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 |
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