VENOVO VENOUS STENT SYSTEM VENEM14140

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a foreign,health professional,s report with the FDA on 2019-07-24 for VENOVO VENOUS STENT SYSTEM VENEM14140 manufactured by Angiomed Gmbh & Co. Medizintechnik Kg.

MAUDE Entry Details

Report Number9681442-2019-00137
MDR Report Key8822732
Report SourceFOREIGN,HEALTH PROFESSIONAL,S
Date Received2019-07-24
Date of Report2019-07-24
Date of Event2019-06-26
Date Mfgr Received2019-06-27
Device Manufacturer Date2016-02-05
Date Added to Maude2019-07-24
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 ContactJUDITH LUDWIG
Manufacturer Street1625 W 3RD ST.
Manufacturer CityTEMPE AZ 85281
Manufacturer CountryUS
Manufacturer Postal85281
Manufacturer Phone4803032689
Manufacturer G1ANGIOMED GMBH & CO. MEDIZINTECHNIK KG
Manufacturer StreetWACHHAUSSTRASSE 6
Manufacturer CityKARLSRUHE 76227
Manufacturer CountryGM
Manufacturer Postal Code76227
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameVENOVO VENOUS STENT SYSTEM
Generic NameVENOUS STENT SYSTEM
Product CodeQAN
Date Received2019-07-24
Catalog NumberVENEM14140
Lot NumberANAY0263
Device Expiration Date2018-01-27
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerANGIOMED GMBH & CO. MEDIZINTECHNIK KG
Manufacturer AddressWACHHAUSSTRASSE 6 KARLSRUHE 76227 GM 76227


Patients

Patient NumberTreatmentOutcomeDate
101. Hospitalization 2019-07-24

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