COMPELLA CAP US SCALE PD PPM P7800A000001

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2019-06-03 for COMPELLA CAP US SCALE PD PPM P7800A000001 manufactured by Hill-rom Batesville.

MAUDE Entry Details

Report Number1824206-2019-00225
MDR Report Key8662538
Date Received2019-06-03
Date of Report2019-05-22
Date of Event2019-05-22
Date Mfgr Received2019-05-22
Device Manufacturer Date2016-07-27
Date Added to Maude2019-06-03
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 ContactEMILY MITCHELL
Manufacturer Street1069 STATE ROUTE 46 EAST
Manufacturer CityBATESVILLE IN 47006
Manufacturer CountryUS
Manufacturer Postal47006
Manufacturer Phone8129310130
Single Use3
Previous Use Code3
Event Type3
Type of Report0

Device Details

Brand NameCOMPELLA CAP US SCALE PD PPM
Generic NameBARIATRIC BED
Product CodeOSI
Date Received2019-06-03
Model NumberP7800A000001
Device AvailabilityY
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerHILL-ROM BATESVILLE
Manufacturer Address1069 STATE ROUTE 46 EAST BATESVILLE IN 47006 US 47006


Patients

Patient NumberTreatmentOutcomeDate
10 2019-06-03

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