ROTOPRONE 209500

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,other report with the FDA on 2019-09-02 for ROTOPRONE 209500 manufactured by Arjohuntleigh, Inc..

MAUDE Entry Details

Report Number9681684-2019-00070
MDR Report Key8953777
Report SourceCOMPANY REPRESENTATIVE,OTHER
Date Received2019-09-02
Date of Report2019-10-01
Date of Event2019-07-01
Date Mfgr Received2019-08-05
Date Added to Maude2019-09-02
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationRISK MANAGER
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactMS. KINGA STOLINSKA
Manufacturer StreetUL. KS. WAWRZYNIAKA 2
Manufacturer CityKOMORNIKI, 62-052, P
Manufacturer CountryPL
Manufacturer Postal62-052, PL
Manufacturer G1ARJOHUNTLEIGH, INC.
Manufacturer Street4958 STOUT DRIVE
Manufacturer CitySAN ANTONIO TX 78219
Manufacturer CountryUS
Manufacturer Postal Code78219
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameROTOPRONE
Generic NameBED, PATIENT ROTATION, POWERED
Product CodeIKZ
Date Received2019-09-02
Model Number209500
OperatorHEALTH PROFESSIONAL
Device Availability*
Device AgeDA
Device Eval'ed by Mfgr*
Device Sequence No1
Device Event Key0
ManufacturerARJOHUNTLEIGH, INC.
Manufacturer Address4958 STOUT DRIVE SAN ANTONIO TX 78219 US 78219


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2019-09-02

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