OG TDL CMPLX FILL COIL 4X12 640CF0412

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,foreig report with the FDA on 2020-03-17 for OG TDL CMPLX FILL COIL 4X12 640CF0412 manufactured by Medos International Sarl.

MAUDE Entry Details

Report Number1226348-2020-00014
MDR Report Key9844587
Report SourceCOMPANY REPRESENTATIVE,FOREIG
Date Received2020-03-17
Date of Report2020-02-25
Date of Event2019-10-13
Date Mfgr Received2020-03-20
Device Manufacturer Date2019-03-06
Date Added to Maude2020-03-17
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. GABRIEL ALFAGEME
Manufacturer Street31 TECHNOLOGY DRIVE
Manufacturer CityIRVINE CA 92618
Manufacturer CountryUS
Manufacturer Postal92618
Manufacturer Phone949789-868
Manufacturer G1CODMAN & SHURTLEFF, INC. (JUAREZ)
Manufacturer StreetCIRCUITO INTERIOR NORTE #1820 PARQUE INDUSTRIAL SALVARCAR
Manufacturer CityJUAREZ CHIHUAHUA 32574
Manufacturer CountryMX
Manufacturer Postal Code32574
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameOG TDL CMPLX FILL COIL 4X12
Generic NameNEUROVASCULAR EMBOLIZATION DEVICE
Product CodeKRD
Date Received2020-03-17
Returned To Mfg2020-03-20
Model Number640CF0412
Catalog Number640CF0412
Lot Number30201509
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device AgeDA
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerMEDOS INTERNATIONAL SARL
Manufacturer AddressCHEMIN-BLANC 38 LE LOCLE MA CH-2400 SZ CH-2400


Patients

Patient NumberTreatmentOutcomeDate
10 2020-03-17

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