23G MST MICRO-HOLDING FORCEPS DFH-0019

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a distributor,foreign report with the FDA on 2019-11-07 for 23G MST MICRO-HOLDING FORCEPS DFH-0019 manufactured by Microsurgical Technology.

MAUDE Entry Details

Report Number3019924-2019-00008
MDR Report Key9291601
Report SourceDISTRIBUTOR,FOREIGN
Date Received2019-11-07
Date of Report2019-11-07
Date of Event2019-09-26
Date Mfgr Received2019-10-08
Device Manufacturer Date2019-01-04
Date Added to Maude2019-11-07
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. CECIL CHRISINGER
Manufacturer Street8415 154TH AVE NE
Manufacturer CityREDMOND WA 98052
Manufacturer CountryUS
Manufacturer Postal98052
Manufacturer Phone4252843754
Manufacturer G1MICROSURGICAL TECHNOLOGY
Manufacturer Street8415 154TH AVE NE
Manufacturer CityREDMOND WA 98052
Manufacturer CountryUS
Manufacturer Postal Code98052
Single Use3
Remedial ActionRL
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand Name23G MST MICRO-HOLDING FORCEPS
Generic NameFORCEPS, OPHTHALMIC
Product CodeHNR
Date Received2019-11-07
Model NumberDFH-0019
Catalog NumberDFH-0019
Lot Number105413
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerMICROSURGICAL TECHNOLOGY
Manufacturer Address8415 154TH AVE NE REDMOND WA 98052 US 98052


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2019-11-07

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