| Primary Device ID | 10848782042828 |
| NIH Device Record Key | ee6d67ba-506c-44b1-90f9-2d9acbd52c2d |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Noevia |
| Version Model Number | LENE07DC |
| Catalog Number | LENE07DC |
| Company DUNS | 812762226 |
| Company Name | Surgical Specialties México, S. de R.L. de C.V. |
| Device Count | 1 |
| DM Exempt | true |
| 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 Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00848782042821 [Primary] |
| GS1 | 10848782042828 [Package] Contains: 00848782042821 Package: Box [12 Units] In Commercial Distribution |
| GAW | Suture, nonabsorbable, synthetic, polypropylene |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2021-11-01 |
| Device Publish Date | 2021-10-22 |
| 20705031227634 - Stratafix Spiral | 2023-12-25 PS-2 2-0 MONODERM 60CM |
| 20705031227986 - Stratafix Spiral | 2023-12-25 PS-2 3-0 MONODERM 30CM |
| 20705031227993 - Stratafix Spiral | 2023-12-25 CT-1 0 MONODERM 45CM |
| 20705031228006 - Stratafix Spiral | 2023-12-25 PS-2 3-0 MONODERM 60CM |
| 20705031228013 - Stratafix Spiral | 2023-12-25 PS-2 2-0 MONODERM 30CM |
| 20705031228020 - Stratafix Spiral | 2023-12-25 CT-1 1 MONODERM 45CM |
| 20705031228037 - Stratafix Spiral | 2023-12-25 SH 0 MONODERM 20CM |
| 20705031228044 - Stratafix Spiral | 2023-12-25 PS-1 2-0 MONODERM 30CM |