ELECTRIC (E-GURNEY) WHEELED STRETCHER 20582

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a health professional,user faci report with the FDA on 2020-03-17 for ELECTRIC (E-GURNEY) WHEELED STRETCHER 20582 manufactured by Sechrist Industries Inc..

MAUDE Entry Details

Report Number2020676-2020-00005
MDR Report Key9845030
Report SourceHEALTH PROFESSIONAL,USER FACI
Date Received2020-03-17
Date of Report2020-02-26
Date of Event2020-02-26
Date Mfgr Received2020-02-26
Device Manufacturer Date2018-05-16
Date Added to Maude2020-03-17
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationOTHER HEALTH CARE PROFESSIONAL
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactMR. MAJID MASHAYEKH
Manufacturer Street4225 E. LA PALMA AVE.
Manufacturer CityANAHEIM, CA
Manufacturer CountryUS
Manufacturer G1SECHRIST INDUSTRIES INC.
Manufacturer Street4225 E. LA PALMA AVENUE
Manufacturer CityANAHEIM, CA
Manufacturer CountryUS
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameELECTRIC (E-GURNEY) WHEELED STRETCHER
Generic NameSTRETCHER, WHEELED,
Product CodeFPO
Date Received2020-03-17
Model Number20582
Catalog Number20582
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerSECHRIST INDUSTRIES INC.
Manufacturer Address4225 E. LA PALMA AVENUE ANAHEIM, CA US


Patients

Patient NumberTreatmentOutcomeDate
10 2020-03-17

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