MALYUGIN RING SYSTEM MAL-0002-1

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 05,06,08 report with the FDA on 2014-12-10 for MALYUGIN RING SYSTEM MAL-0002-1 manufactured by Microsurgical Technology, Inc..

Event Text Entries

[5199661] The user facility reported to the distributor that the malyugin ring tore a capsule when being inserted into the pupillary margin. The surgeon was able to salvage the capsular bag and implant and iol without further impact to the pt.
Patient Sequence No: 1, Text Type: D, B5


[12697261] The eval on the returned device was inconclusive. The cause of the capsular tear is unk.
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number3019924-2014-00056
MDR Report Key4346067
Report Source05,06,08
Date Received2014-12-10
Date of Report2014-12-05
Date Mfgr Received2014-11-11
Date Added to Maude2014-12-22
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 FDA0
Event Location0
Manufacturer Street8415 154TH AVE., N.E.
Manufacturer CityREDMOND WA 98052
Manufacturer CountryUS
Manufacturer Postal98052
Manufacturer Phone4255560544
Single Use3
Remedial ActionRL
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameMALYUGIN RING SYSTEM
Generic NameIRIS CLIP RETRACTOR
Product CodeHOC
Date Received2014-12-10
Returned To Mfg2014-11-26
Model NumberMAL-0002-1
Catalog NumberMAL-0002-1
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device AgeDA
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerMICROSURGICAL TECHNOLOGY, INC.
Manufacturer AddressREDMOND WA US


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2014-12-10

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