CODMAN NEEDLE HOLDER 36-2017

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2019-07-23 for CODMAN NEEDLE HOLDER 36-2017 manufactured by Codman / Symmetry Surgical Gmbh.

MAUDE Entry Details

Report NumberMW5088311
MDR Report Key8821941
Date Received2019-07-23
Date of Report2019-07-19
Date of Event2019-07-16
Date Added to Maude2019-07-24
Event Key0
Report Source CodeVoluntary report
Manufacturer LinkN
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationRISK MANAGER
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Single Use3
Previous Use Code3
Event Type3
Type of Report0

Device Details

Brand NameCODMAN NEEDLE HOLDER
Generic NameFORCEPS, GENERAL & PLASTIC SURGERY
Product CodeGEN
Date Received2019-07-23
Catalog Number36-2017
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device Eval'ed by MfgrI
Device Sequence No1
Device Event Key0
ManufacturerCODMAN / SYMMETRY SURGICAL GMBH
Manufacturer AddressUS


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2019-07-23

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