• Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

MAUDE Adverse Event Report: JIANGSU YUYUE MEDICAL EQUIPMENT & SUPPLY CO., LTD HVY DUTY TRANSPORT 22 IN-W/FTRST 9153643753; WHEELCHAIR, MECHANICAL

  • Print
  • Share
  • E-mail
-
Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 

JIANGSU YUYUE MEDICAL EQUIPMENT & SUPPLY CO., LTD HVY DUTY TRANSPORT 22 IN-W/FTRST 9153643753; WHEELCHAIR, MECHANICAL Back to Search Results
Model Number TRHD22FR
Device Problem Torn Material (3024)
Patient Problem No Consequences Or Impact To Patient (2199)
Event Type  malfunction  
Event Description
Dealer states the seat upholstery is tearing at the seam on the right side.
 
Search Alerts/Recalls

  New Search  |  Submit an Adverse Event Report

Brand Name
HVY DUTY TRANSPORT 22 IN-W/FTRST 9153643753
Type of Device
WHEELCHAIR, MECHANICAL
Manufacturer (Section D)
JIANGSU YUYUE MEDICAL EQUIPMENT & SUPPLY CO., LTD
yunyang industrial park
danyang city
jiangsu pro
CH 
MDR Report Key4431432
MDR Text Key21838073
Report Number1531186-2015-00377
Device Sequence Number1
Product Code IOR
Combination Product (y/n)N
Reporter Country CodeUS
Number of Events Reported1
Summary Report (Y/N)N
Report Source Distributor
Source Type Invalid Data
Reporter Occupation Medical Equipment Company Technician/Representative
Type of Report Initial
Report Date 01/16/2015,01/08/2015
1 Device was Involved in the Event
1 Patient was Involved in the Event
Date FDA Received01/20/2015
Is this an Adverse Event Report? No
Is this a Product Problem Report? Yes
Device Operator Lay User/Patient
Device Model NumberTRHD22FR
Was Device Available for Evaluation? No
Is the Reporter a Health Professional? No
Was the Report Sent to FDA? Yes
Date Report Sent to FDA01/16/2015
Distributor Facility Aware Date01/08/2015
Device Age11 MO
Date Report to Manufacturer01/16/2015
Is This a Reprocessed and Reused Single-Use Device? No
Patient Sequence Number1
Patient Outcome(s) Other;
-
-