| Primary Device ID | B772DWB2101 |
| NIH Device Record Key | 56daa731-ff8e-4589-a0d5-2cd820e3240e |
| Commercial Distribution Discontinuation | 2024-06-24 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | SCREWCOG |
| Version Model Number | 20X1 |
| Catalog Number | DWB-21-01 |
| Company DUNS | 465769007 |
| Company Name | MEDYGLOBAL MEDICAL DEVICES SL. |
| Device Count | 20 |
| 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 | true |
| Manufacturing Date | true |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | true |
| RX Perscription | false |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| HIBCC | B772DWB2101 [Primary] |
| HIBCC | SCREWCOGDWB2101 [Unit of Use] |
| NEW | Suture, Surgical, Absorbable, Polydioxanone |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2021-06-15 |
| Device Publish Date | 2021-06-07 |
| B772DWB2102 | PDO THREADS WITH BIOABSORBABLE MATERIAL WITH NEEDLE |
| B772DWB2101 | PDO THREADS BIOABSORBABLE MATERIAL WITH NEEDLE |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() SCREWCOG 79334090 not registered Live/Pending |
MEDYGLOBAL MEDICAL DEVICES, S.L. 2021-11-11 |