PARKER BATH AL14110-US

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,user f report with the FDA on 2019-08-14 for PARKER BATH AL14110-US manufactured by Arjo Hospital Equipment Ab.

MAUDE Entry Details

Report Number3007420694-2019-00134
MDR Report Key8891951
Report SourceCOMPANY REPRESENTATIVE,USER F
Date Received2019-08-14
Date of Report2019-09-13
Date of Event2019-07-01
Date Mfgr Received2019-07-29
Device Manufacturer Date2006-10-09
Date Added to Maude2019-08-14
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 ContactMS. KINGA STOLINSKA
Manufacturer StreetKS. WAWRZYNIAKA 2
Manufacturer CityKOMORNIKI, 62-052
Manufacturer CountryPL
Manufacturer Postal62-052
Manufacturer G1ARJO HOSPITAL EQUIPMENT AB
Manufacturer StreetVERKSTADSVAGEN 5
Manufacturer CityESLOV, 24121
Manufacturer CountrySW
Manufacturer Postal Code24121
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NamePARKER BATH
Generic NameBATH, HYDRO-MASSAGE
Product CodeILJ
Date Received2019-08-14
Model NumberAL14110-US
Device AvailabilityY
Device AgeDA
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerARJO HOSPITAL EQUIPMENT AB
Manufacturer AddressVERKSTADSVAGEN 5 ESLOV, 24121 SW 24121


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2019-08-14

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.