| Primary Device ID | 10848782029218 |
| NIH Device Record Key | 98af51f4-892e-433c-a35c-e69b1047f95e |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | CyberTech |
| Version Model Number | 900-8113 |
| 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 Issuing Agency | Device ID |
|---|---|
| GS1 | 00848782029211 [Primary] |
| GS1 | 10848782029218 [Package] Contains: 00848782029211 Package: Box [12 Units] In Commercial Distribution |
| GAM | SUTURE, ABSORBABLE, SYNTHETIC, POLYGLYCOLIC ACID |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2019-03-11 |
| Device Publish Date | 2019-02-19 |
| 10848782029379 | C7 3-0 BBS 18"/45CM |
| 10848782029362 | C7 2-0 BBS 18"/45CM |
| 10848782029355 | C6 4-0 BBS 18"/45CM |
| 10848782029348 | C6 3-0 BBS 18"/45CM |
| 10848782029331 | C22 5-0 BBS 18"/45CM |
| 10848782029324 | C22 4-0 BBS 18"/45CM |
| 10848782029317 | C22 3-0 BBS 18"/45CM |
| 10848782029300 | C17 5-0 BBS 18"/45CM |
| 10848782029294 | C3P 4-0 BBS 18"/45CM |
| 10848782029287 | T14 3-0 BBS 18"/45CM |
| 10848782029270 | C9 3-0 BBS 18"/45CM |
| 10848782029263 | C20 4-0 BBS 18"/45CM |
| 10848782029256 | HS16 3-0 BBS 18"/45CM |
| 10848782029249 | C7 3-0 VIO BR PGA 27/70 |
| 10848782029232 | C6 4-0 VIO BR PGA 27/70 |
| 10848782029225 | T28 4-0 VIO BR PGA 18/45 |
| 10848782029218 | C6 4-0 UNDYED BR PGA-FA 18/45 |
| 10848782029201 | C6 3-0 UNDYED BR PGA-FA 18/45 |