COMPACT DELTA II K1026730

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2020-03-12 for COMPACT DELTA II K1026730 manufactured by Dornier Medtech Systems Gmbh.

Event Text Entries

[183114250] A service report completed 03/02/2020 by a dmta field service engineer concluded that the device was operating within dornier specifications. A hematoma is listed as a potential adverse effect and complication in the compact delta ii operating manual. The details concerning individual patient outcome are not known beyond treatment for the noted hematoma. No defects or inconsistencies were noted with the device as manufactured. No fault was identified with the device during this investigation.
Patient Sequence No: 1, Text Type: N, H10


[183114251] Patient hematoma reported.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1037955-2020-00006
MDR Report Key9823855
Date Received2020-03-12
Date of Report2020-02-28
Date Facility Aware2020-02-28
Report Date2020-03-03
Date Reported to Mfgr2020-03-03
Date Added to Maude2020-03-12
Event Key0
Report Source CodeDistributor report
Manufacturer LinkN
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
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameCOMPACT DELTA II
Generic NameLITHOTRIPTER
Product CodeLNS
Date Received2020-03-12
Model NumberCOMPACT DELTA II
Catalog NumberK1026730
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device Age15 YR
Device Eval'ed by Mfgr*
Device Sequence No1
Device Event Key0
ManufacturerDORNIER MEDTECH SYSTEMS GMBH
Manufacturer AddressARGELSRIEDER FELD 7 WESSLING, D-82234 GM D-82234


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2020-03-12

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