UNK

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2003-08-25 for UNK manufactured by Unk.

Event Text Entries

[18146961] Removal of 2 k-wires.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number480407
MDR Report Key480407
Date Received2003-08-25
Date of Report2003-08-25
Date of Event2003-08-07
Date Facility Aware2003-08-07
Report Date2003-08-25
Date Reported to FDA2003-08-25
Date Added to Maude2003-08-29
Event Key0
Report Source CodeUser Facility report
Manufacturer LinkN
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag0
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Single Use0
Previous Use Code0
Event Type3
Type of Report3

Device Details

Brand NameUNK
Generic NameUNK
Product CodeDZK
Date Received2003-08-25
Model NumberUNK
Catalog NumberUNK
Lot NumberUNK
ID NumberUNK
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device AgeUNKNOWN
Implant FlagY
Date RemovedV
Device Sequence No1
Device Event Key469254
ManufacturerUNK
Manufacturer AddressUNK UNK *


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2003-08-25

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