MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,health report with the FDA on 2019-11-20 for PLAIN GUT G-1774-K manufactured by Davis & Geck Caribe Ltd.
Report Number | 9612501-2019-02239 |
MDR Report Key | 9347111 |
Report Source | COMPANY REPRESENTATIVE,HEALTH |
Date Received | 2019-11-20 |
Date of Report | 2019-11-20 |
Date of Event | 2019-10-26 |
Date Mfgr Received | 2019-11-04 |
Date Added to Maude | 2019-11-20 |
Event Key | 0 |
Report Source Code | Manufacturer report |
Manufacturer Link | Y |
Number of Patients in Event | 0 |
Adverse Event Flag | 3 |
Product Problem Flag | 3 |
Reprocessed and Reused Flag | 3 |
Reporter Occupation | OTHER HEALTH CARE PROFESSIONAL |
Health Professional | 3 |
Initial Report to FDA | 3 |
Report to FDA | 3 |
Event Location | 3 |
Manufacturer Contact | LISA HERNANDEZ |
Manufacturer Street | 60 MIDDLETOWN AVE. |
Manufacturer City | NORTH HAVEN CT 06473 |
Manufacturer Country | US |
Manufacturer Postal | 06473 |
Manufacturer Phone | 2034925563 |
Manufacturer G1 | DAVIS & GECK CARIBE LTD |
Manufacturer Street | ZONA FRANCA DE SAN ISIDRO |
Manufacturer City | SANTO DOMINGO 0101 |
Manufacturer Country | DO |
Manufacturer Postal Code | 0101 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | PLAIN GUT |
Generic Name | SUTURE, ABSORBABLE, NATURAL |
Product Code | GAL |
Date Received | 2019-11-20 |
Model Number | G-1774-K |
Catalog Number | G-1774-K |
Operator | HEALTH PROFESSIONAL |
Device Availability | N |
Device Eval'ed by Mfgr | * |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | DAVIS & GECK CARIBE LTD |
Manufacturer Address | ZONA FRANCA DE SAN ISIDRO SANTO DOMINGO 0101 DO 0101 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Required No Informationntervention | 2019-11-20 |