| Primary Device ID | 00812337027076 | 
| NIH Device Record Key | eff462ca-64cf-49f7-9077-39b1ba2b5993 | 
| Commercial Distribution Discontinuation | 2019-09-30 | 
| Commercial Distribution Status | Not in Commercial Distribution | 
| Brand Name | OptiMatrix™ Extracellular Matrix | 
| Version Model Number | 30053-01 | 
| Catalog Number | 40-1520 | 
| 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 | 
| Width | 15 Millimeter | 
| Width | 15 Millimeter | 
| Width | 15 Millimeter | 
| Width | 15 Millimeter | 
| Length | 20 Millimeter | 
| Width | 15 Millimeter | 
| Length | 20 Millimeter | 
| Width | 15 Millimeter | 
| Length | 20 Millimeter | 
| Width | 15 Millimeter | 
| Length | 20 Millimeter | 
| Width | 15 Millimeter | 
| Length | 20 Millimeter | 
| Width | 15 Millimeter | 
| Length | 20 Millimeter | 
| Width | 15 Millimeter | 
| Length | 20 Millimeter | 
| Width | 15 Millimeter | 
| Length | 20 Millimeter | 
| Width | 15 Millimeter | 
| Length | 20 Millimeter | 
| Width | 15 Millimeter | 
| Length | 20 Millimeter | 
| Width | 15 Millimeter | 
| Length | 20 Millimeter | 
| Width | 15 Millimeter | 
| Length | 20 Millimeter | 
| Width | 15 Millimeter | 
| Length | 20 Millimeter | 
| Width | 15 Millimeter | 
| Length | 20 Millimeter | 
| Width | 15 Millimeter | 
| Length | 20 Millimeter | 
| Width | 15 Millimeter | 
| Length | 20 Millimeter | 
| Width | 15 Millimeter | 
| Device Issuing Agency | Device ID | 
|---|---|
| GS1 | 00812337027076 [Primary] | 
| NPL | Barrier, Animal Source, Intraoral | 
| Steralize Prior To Use | false | 
| Device Is Sterile | true | 
| Public Version Status | Update | 
| Device Record Status | Published | 
| Public Version Number | 4 | 
| Public Version Date | 2019-10-01 | 
| Device Publish Date | 2015-09-16 | 
| 00812337027090 | 30053-03 | 
| 00812337027083 | 30053-02 | 
| 00812337027076 | 30053-01 | 
| 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 |