ORCHESTRA

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 2020-02-03 for ORCHESTRA manufactured by Sorin Group Italia S.r.l. - Crm Facility.

Event Text Entries

[181819778] Reportedly, the subject programmer takes a long time to interrogate a device and then freezes.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1000165971-2020-00248
MDR Report Key9662452
Report SourceCOMPANY REPRESENTATIVE
Date Received2020-02-03
Date of Report2020-03-17
Date of Event2020-01-09
Date Facility Aware2020-01-09
Date Mfgr Received2020-02-21
Date Added to Maude2020-02-03
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 ContactLAURA OUAKI
Manufacturer StreetPARC D'AFFAIRES NOVEOS 4 AVENUE R .
Manufacturer CityCLAMART 92140
Manufacturer CountryFR
Manufacturer Postal92140
Manufacturer Phone146013429
Manufacturer G1GESPAC 18, CHEMIN DES AULX CH-1228 GEN
Manufacturer StreetPARC D'AFFAIRES NOVEOS 4 AVENUE R .
Manufacturer CityCLAMART 92140
Manufacturer CountryFR
Manufacturer Postal Code92140
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameORCHESTRA
Generic NamePROGRAMMER, PACEMAKER
Product CodeMRM
Date Received2020-02-03
Returned To Mfg2020-01-20
Model NumberORCHESTRA
Catalog NumberORCHESTRA
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device AgeDA
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerSORIN GROUP ITALIA S.R.L. - CRM FACILITY
Manufacturer AddressPARC D'AFFAIRES NOVEOS 4 AVENUE R?AUMUR . CLAMART 92140 FR 92140


Patients

Patient NumberTreatmentOutcomeDate
10 2020-02-03

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