MALYUGIN RING SYSTEM MAL-0002

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2017-02-21 for MALYUGIN RING SYSTEM MAL-0002 manufactured by Microsurgical Technology Inc.

Event Text Entries

[67928648] The device was discarded and not returned for evaluation. The complaint could not be confirmed.
Patient Sequence No: 1, Text Type: N, H10


[67928649] The surgeon reported that an iris retractor had torn a part of the iris causing an iridodialysis and iris hyphema upon removal from the eye.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number3019924-2017-00002
MDR Report Key6347809
Date Received2017-02-21
Date of Report2017-02-20
Date Mfgr Received2017-01-31
Date Added to Maude2017-02-21
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationMEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactMR. JOHN RAY
Manufacturer Street8415 154TH AVE NE
Manufacturer CityREDMOND WA 98052
Manufacturer CountryUS
Manufacturer Postal98052
Manufacturer Phone4255560544
Manufacturer G1MICROSURGICAL TECHNOLOGY INC
Manufacturer Street8415 154TH AVE NE
Manufacturer CityREDMOND WA 98052
Manufacturer CountryUS
Manufacturer Postal Code98052
Single Use3
Previous Use Code3
Event Type3
Type of Report0

Device Details

Brand NameMALYUGIN RING SYSTEM
Generic NameIRISI RETRACTOR CLIP
Product CodeHOC
Date Received2017-02-21
Model NumberMAL-0002
Catalog NumberMAL-0002
OperatorPHYSICIAN
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerMICROSURGICAL TECHNOLOGY INC
Manufacturer Address8415 154TH AVE NE REDMOND WA 98052 US 98052


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2017-02-21

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