ARTICULATING ARM OF EMPOWER CTA 017417 800840-003

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2019-06-19 for ARTICULATING ARM OF EMPOWER CTA 017417 800840-003 manufactured by Bracco Injeneering S.a..

MAUDE Entry Details

Report Number3004753774-2019-00002
MDR Report Key8711969
Date Received2019-06-19
Date of Report2019-05-23
Date of Event2019-05-18
Date Mfgr Received2019-05-23
Date Added to Maude2019-06-19
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationOTHER HEALTH CARE PROFESSIONAL
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactCEDRIC BOESCH
Manufacturer Street46 AVENUE SEVELIN
Manufacturer CityLAUSANNE, CH-1004
Manufacturer CountrySZ
Manufacturer PostalCH-1004
Manufacturer G1BRACCO INJENEERING S.A.
Manufacturer Street46 AVENUE SEVELIN
Manufacturer CityLAUSANNE, CH-1004
Manufacturer CountrySZ
Manufacturer Postal CodeCH-1004
Single Use3
Previous Use Code3
Event Type3
Type of Report0

Device Details

Brand NameARTICULATING ARM OF EMPOWER CTA
Generic NameARTICULATING ARM OF EMPOWER CTA
Product CodeIZQ
Date Received2019-06-19
Model Number017417
Catalog Number800840-003
Device AvailabilityY
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerBRACCO INJENEERING S.A.
Manufacturer Address46 AVENUE SEVELIN LAUSANNE, CH-1004 SZ CH-1004


Patients

Patient NumberTreatmentOutcomeDate
10 2019-06-19

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