LIFESTREAM BALLOON EXPANDABLE VASCULAR COVERED STENT LSMU0800737

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative report with the FDA on 2019-08-02 for LIFESTREAM BALLOON EXPANDABLE VASCULAR COVERED STENT LSMU0800737 manufactured by Clearstream Technologies Ltd..

MAUDE Entry Details

Report Number9616666-2019-00088
MDR Report Key8855130
Report SourceCOMPANY REPRESENTATIVE
Date Received2019-08-02
Date of Report2019-08-02
Date Mfgr Received2019-07-08
Device Manufacturer Date2018-06-07
Date Added to Maude2019-08-02
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 G1CLEARSTREAM TECHNOLOGIES LTD.
Manufacturer StreetMOYNE UPPER
Manufacturer CityENNISCORTHY, CO. WEXFORD
Manufacturer CountryEI
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameLIFESTREAM BALLOON EXPANDABLE VASCULAR COVERED STENT
Generic NameBALLOON EXPANDABLE VASCULAR COVERED STENT
Product CodePRL
Date Received2019-08-02
Model NumberLSMU0800737
Catalog NumberLSMU0800737
Lot NumberCMCT0058
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerCLEARSTREAM TECHNOLOGIES LTD.
Manufacturer AddressMOYNE UPPER ENNISCORTHY, CO. WEXFORD EI


Patients

Patient NumberTreatmentOutcomeDate
10 2019-08-02

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