AFFINITY 4 BED FRAME P3700E000030

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2019-09-03 for AFFINITY 4 BED FRAME P3700E000030 manufactured by Hill-rom Batesville.

MAUDE Entry Details

Report Number1824206-2019-00337
MDR Report Key8958056
Date Received2019-09-03
Date of Report2019-08-22
Date of Event2019-08-22
Date Mfgr Received2019-08-22
Device Manufacturer Date2018-08-06
Date Added to Maude2019-09-03
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 ContactLORI DAULTON
Manufacturer Street1069 STATE ROUTE 46 EAST
Manufacturer CityBATESVILLE IN 47006
Manufacturer CountryUS
Manufacturer Postal47006
Manufacturer Phone8129312280
Single Use3
Previous Use Code3
Event Type3
Type of Report0

Device Details

Brand NameAFFINITY 4 BED FRAME
Generic NameTABLE, OBSTETRIC
Product CodeKNC
Date Received2019-09-03
Model NumberP3700E000030
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerHILL-ROM BATESVILLE
Manufacturer Address1069 STATE ROUTE 46 EAST BATESVILLE IN 47006 US 47006


Patients

Patient NumberTreatmentOutcomeDate
10 2019-09-03

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