| Primary Device ID | 00616784914237 |
| NIH Device Record Key | 0c2e021c-454c-41dd-b1ef-459e0c21664f |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Silk Sutures |
| Version Model Number | 9142 |
| Company DUNS | 008124539 |
| Company Name | DYNAREX CORPORATION |
| Device Count | 12 |
| 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 | true |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | false |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00616784914213 [Unit of Use] |
| GS1 | 00616784914220 [Primary] |
| GS1 | 00616784914237 [Package] Contains: 00616784914220 Package: [25 Units] In Commercial Distribution |
| GS1 | 00840117346420 [Package] Contains: 00616784914213 Package: Box [12 Units] In Commercial Distribution |
| GAP | Suture, Nonabsorbable, Silk |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2016-09-24 |
| 00616784914336 | 9143 |
| 00616784914237 | 9142 |