| Primary Device ID | 00812337023719 | 
| NIH Device Record Key | ad961b71-60dd-4e40-9370-5bf1606704da | 
| Commercial Distribution Status | In Commercial Distribution | 
| Brand Name | TrelliForm | 
| Version Model Number | 30017-01 | 
| Catalog Number | TF0612 | 
| 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 | 6 Centimeter | 
| Length | 12 Centimeter | 
| Width | 6 Centimeter | 
| Length | 12 Centimeter | 
| Width | 6 Centimeter | 
| Length | 12 Centimeter | 
| Width | 6 Centimeter | 
| Length | 12 Centimeter | 
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| Length | 12 Centimeter | 
| Width | 6 Centimeter | 
| Length | 12 Centimeter | 
| Width | 6 Centimeter | 
| Device Issuing Agency | Device ID | 
|---|---|
| GS1 | 00812337023719 [Primary] | 
| FTM | Mesh, Surgical | 
| Steralize Prior To Use | false | 
| Device Is Sterile | true | 
| Public Version Status | New | 
| Device Record Status | Published | 
| Public Version Number | 1 | 
| Public Version Date | 2019-10-15 | 
| Device Publish Date | 2019-10-07 | 
| 00812337023771 | 30017-07 | 
| 00812337023764 | 30017-06 | 
| 00812337023757 | 30017-05 | 
| 00812337023740 | 30017-04 | 
| 00812337023733 | 30017-03 | 
| 00812337023726 | 30017-02 | 
| 00812337023719 | 30017-01 | 
| Mark Image Registration | Serial | Company Trademark Application Date | 
|---|---|
|  TRELLIFORM  87540086  5938513 Live/Registered | CorsaMed 2017-07-24 |