MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a health professional report with the FDA on 2019-10-11 for DIGITEX SUTURE DELIVERY DEVICE 5202501022 520250 manufactured by Coloplast Corp.
Report Number | 2125050-2019-00860 |
MDR Report Key | 9181805 |
Report Source | HEALTH PROFESSIONAL |
Date Received | 2019-10-11 |
Date of Report | 2019-10-08 |
Date of Event | 2019-09-02 |
Date Mfgr Received | 2019-09-12 |
Date Added to Maude | 2019-10-11 |
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 |
Health Professional | 0 |
Initial Report to FDA | 0 |
Report to FDA | 3 |
Event Location | 3 |
Manufacturer Contact | STEPHANIE PERRYMAN |
Manufacturer Street | 1601 WEST RIVIER ROAD NORTH |
Manufacturer City | MINNEAPOLIS MN 55411 |
Manufacturer Country | US |
Manufacturer Postal | 55411 |
Manufacturer Phone | 6124345685 |
Manufacturer G1 | COLOPLAST MANUFACTURING US, LLC |
Manufacturer Street | 1601 WEST RIVIER ROAD NORTH |
Manufacturer City | MINNEAPOLIS MN 55411 |
Manufacturer Country | US |
Manufacturer Postal Code | 55411 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | DIGITEX SUTURE DELIVERY DEVICE |
Generic Name | INSTRUMENTATION FOR USE WITH UROGYNECOLOGIC SURGICAL MESH |
Product Code | PWI |
Date Received | 2019-10-11 |
Returned To Mfg | 2019-10-01 |
Model Number | 5202501022 |
Catalog Number | 520250 |
Lot Number | 6596856 |
Operator | HEALTH PROFESSIONAL |
Device Availability | R |
Device Eval'ed by Mfgr | N |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | COLOPLAST CORP |
Manufacturer Address | 1601 WEST RIVIER ROAD NORTH MINNEAPOLIS MN 55411 US 55411 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Other | 2019-10-11 |