ORSIRO 3.0/26 364508 SEE MODEL NO.

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 2020-03-30 for ORSIRO 3.0/26 364508 SEE MODEL NO. manufactured by Biotronik Ag, Buelach, Switzerland.

Event Text Entries

[185702548] An orsiro drug-eluting stent system was selected for treatment. After placement of the device in the pre-dilated target lesion it was noticed that the stent is not on the balloon. The stent was found outside patient on the transportation wire.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1028232-2020-01459
MDR Report Key9901519
Report SourceCOMPANY REPRESENTATIVE,FOREIG
Date Received2020-03-30
Date of Report2020-03-25
Date of Event2020-02-28
Date Mfgr Received2020-03-25
Device Manufacturer Date2019-09-25
Date Added to Maude2020-03-30
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 Street6024 JEAN ROAD
Manufacturer CityLAKE OSWEGO OR 97035
Manufacturer CountryUS
Manufacturer Postal97035
Manufacturer Phone8772459800
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameORSIRO 3.0/26
Generic NameCORONARY DRUG-ELUTING STENT
Product CodeNIQ
Date Received2020-03-30
Returned To Mfg2020-03-10
Model Number364508
Catalog NumberSEE MODEL NO.
Lot Number09192207
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device Eval'ed by Mfgr*
Device Sequence No1
Device Event Key0
ManufacturerBIOTRONIK AG, BUELACH, SWITZERLAND
Manufacturer AddressACKERSTRASSE 6 BUELACH CH-8180 CH CH-8180


Patients

Patient NumberTreatmentOutcomeDate
10 2020-03-30

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