DIGITEX SUTURE DELIVERY DEVICE 5202501022 520250

MAUDE Adverse Event Report

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.

MAUDE Entry Details

Report Number2125050-2019-00860
MDR Report Key9181805
Report SourceHEALTH PROFESSIONAL
Date Received2019-10-11
Date of Report2019-10-08
Date of Event2019-09-02
Date Mfgr Received2019-09-12
Date Added to Maude2019-10-11
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Health Professional0
Initial Report to FDA0
Report to FDA3
Event Location3
Manufacturer ContactSTEPHANIE PERRYMAN
Manufacturer Street1601 WEST RIVIER ROAD NORTH
Manufacturer CityMINNEAPOLIS MN 55411
Manufacturer CountryUS
Manufacturer Postal55411
Manufacturer Phone6124345685
Manufacturer G1COLOPLAST MANUFACTURING US, LLC
Manufacturer Street1601 WEST RIVIER ROAD NORTH
Manufacturer CityMINNEAPOLIS MN 55411
Manufacturer CountryUS
Manufacturer Postal Code55411
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameDIGITEX SUTURE DELIVERY DEVICE
Generic NameINSTRUMENTATION FOR USE WITH UROGYNECOLOGIC SURGICAL MESH
Product CodePWI
Date Received2019-10-11
Returned To Mfg2019-10-01
Model Number5202501022
Catalog Number520250
Lot Number6596856
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerCOLOPLAST CORP
Manufacturer Address1601 WEST RIVIER ROAD NORTH MINNEAPOLIS MN 55411 US 55411


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2019-10-11

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