STAMEY MALECOT SUPRAPUBIC CATHETER SET 081014

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a foreign,literature,other report with the FDA on 2019-07-01 for STAMEY MALECOT SUPRAPUBIC CATHETER SET 081014 manufactured by Cook Inc.

MAUDE Entry Details

Report Number1820334-2019-01587
MDR Report Key8748840
Report SourceFOREIGN,LITERATURE,OTHER
Date Received2019-07-01
Date of Report2019-07-01
Date of Event1995-02-06
Date Mfgr Received2019-09-19
Date Added to Maude2019-07-01
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactMR. LARRY POOL
Manufacturer Street750 DANIELS WAY
Manufacturer CityBLOOMINGTON IN 47404
Manufacturer CountryUS
Manufacturer Postal47404
Manufacturer Phone8123392235
Manufacturer G1COOK INC
Manufacturer Street750 DANIELS WAY
Manufacturer CityBLOOMINGTON IN 47404
Manufacturer CountryUS
Manufacturer Postal Code47404
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameSTAMEY MALECOT SUPRAPUBIC CATHETER SET
Generic NameKOB CATHETER, SUPRAPUBIC (AND ACCESSORIES)
Product CodeKOB
Date Received2019-07-01
Catalog Number081014
Lot NumberUNKNOWN
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device AgeDA
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerCOOK INC
Manufacturer Address750 DANIELS WAY BLOOMINGTON IN 47404 US 47404


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2019-07-01

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