Primary Device ID | B772DWB2102 |
NIH Device Record Key | e818df32-4ff4-47f4-9729-dfc00931621c |
Commercial Distribution Discontinuation | 2024-06-24 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | SCREWCOG |
Version Model Number | 20X1 |
Catalog Number | 21GX90 |
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 | B772DWB2102 [Primary] |
HIBCC | SCREWCOG21GX90 [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 | 2021-06-14 |
Device Publish Date | 2021-06-04 |
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 |