| Primary Device ID | 03661522103128 |
| NIH Device Record Key | f13aff3d-01e3-4b13-baeb-5072cc72cc1d |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | CARDIONYL® |
| Version Model Number | 72K07K |
| Company DUNS | 265741780 |
| Company Name | PETERS SURGICAL |
| 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 | true |
| 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 Issuing Agency | Device ID |
|---|---|
| GS1 | 03661522103128 [Primary] |
| GAR | Suture, Nonabsorbable, Synthetic, Polyamide |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2026-03-13 |
| Device Publish Date | 2026-03-05 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() CARDIONYL 76535974 2922132 Live/Registered |
PETERS SURGICAL 2003-07-25 |
![]() CARDIONYL 74357874 1967167 Dead/Cancelled |
PETERS LABORATORIES 1993-02-11 |