PRESIDIO 10 CERE 7MMX30CM PC4100730-30 PC410073030

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 2020-03-23 for PRESIDIO 10 CERE 7MMX30CM PC4100730-30 PC410073030 manufactured by Medos International Sarl.

MAUDE Entry Details

Report Number3008114965-2020-00072
MDR Report Key9868342
Report SourceCOMPANY REPRESENTATIVE,FOREIG
Date Received2020-03-23
Date of Report2020-02-26
Date of Event2020-02-24
Date Mfgr Received2020-03-18
Device Manufacturer Date2019-03-12
Date Added to Maude2020-03-23
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. (FREMONT)
Manufacturer Street47709 FREMONT BLVD
Manufacturer CityFREMONT CA 94538
Manufacturer CountryUS
Manufacturer Postal Code94538
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NamePRESIDIO 10 CERE 7MMX30CM
Generic NameNEUROVASCULAR EMBOLIZATION DEVICE
Product CodeHCG
Date Received2020-03-23
Returned To Mfg2020-03-17
Model NumberPC4100730-30
Catalog NumberPC410073030
Lot NumberL15246
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerMEDOS INTERNATIONAL SARL
Manufacturer AddressCHEMIN-BLANC 38 LE LOCLE NEUCHATEL CH-2400 SZ CH-2400


Patients

Patient NumberTreatmentOutcomeDate
10 2020-03-23

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