CUNITI WIRE 205-1902

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2019-02-04 for CUNITI WIRE 205-1902 manufactured by Sds De Mexico.

Event Text Entries

[136993987] A doctor reported to the european distributor that he had wire breakage with being swallowed sometimes. No patient injuries. There was no additional information provided but the product was passed naturally.
Patient Sequence No: 1, Text Type: N, H10


[136993988] The cuniti wires broke and possibly passed naturally. There were no reportable injuries.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number2016150-2019-00002
MDR Report Key8303269
Date Received2019-02-04
Date of Report2019-04-26
Date of Event2019-01-13
Date Mfgr Received2019-01-13
Date Added to Maude2019-02-04
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 ContactMRS. SUZETTE RAMPAIR-JOHNSON
Manufacturer Street1889 W. MISSION BLVD
Manufacturer CityPOMONA CA 91766
Manufacturer CountryUS
Manufacturer Postal91766
Manufacturer Phone9096713431
Manufacturer G1SDS DE MEXICO
Manufacturer StreetS. DE R.L. DE C.V. CIRCUITO SUR NO. 31
Manufacturer CityMEXICALI, MEXICO 21395
Manufacturer CountryMX
Manufacturer Postal Code21395
Single Use3
Previous Use Code3
Event Type3
Type of Report0

Device Details

Brand NameCUNITI WIRE
Generic NameDAMON COPPER NITI WIRE
Product CodeDZC
Date Received2019-02-04
Catalog Number205-1902
Device AvailabilityN
Device AgeDA
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerSDS DE MEXICO
Manufacturer AddressS. DE R.L. C.V. CIRCUITO SUR NO 31 MEXICALI, MEXICO C.P.


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2019-02-04

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