CRAGG MACNAMARA VALVED INFUSION CATHETER * 201-0217

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 1998-10-20 for CRAGG MACNAMARA VALVED INFUSION CATHETER * 201-0217 manufactured by Micro Therapeutics Inc..

Event Text Entries

[19494449] Distal ring of cragg-macnamara 5 french infusion catheter dislodged during removal from a gortex-hemodialysis graft embolized into the radial artery.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report NumberMW1014786
MDR Report Key192735
Date Received1998-10-20
Date Added to Maude1998-10-23
Event Key0
Report Source CodeVoluntary report
Manufacturer LinkN
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag0
Health Professional3
Initial Report to FDA0
Report to FDA0
Event Location3
Single Use0
Previous Use Code0
Event Type3
Type of Report3

Device Details

Brand NameCRAGG MACNAMARA VALVED INFUSION CATHETER
Generic NameINFUSION CATHETER
Product CodeJCY
Date Received1998-10-20
Model Number*
Catalog Number201-0217
Lot Number*
ID Number*
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Implant FlagN
Date Removed*
Device Sequence No1
Device Event Key187278
ManufacturerMICRO THERAPEUTICS INC.
Manufacturer Address1062-F CALLE NEGOCIO SAN CLEMENTE CA 92673 US


Patients

Patient NumberTreatmentOutcomeDate
10 1998-10-20

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