• 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 SHWR COMMODE 23 IN TIRES 16 IN W 9153640950; ADAPTOR, HYGIENE

  • 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 SHWR COMMODE 23 IN TIRES 16 IN W 9153640950; ADAPTOR, HYGIENE Back to Search Results
Model Number 6795
Device Problem Device Inoperable (1663)
Patient Problem No Consequences Or Impact To Patient (2199)
Event Type  malfunction  
Event Description
Dealer is stating that the front casters are not swiveling.Dealer is stating that there is no sign of rust.
 
Search Alerts/Recalls

  New Search  |  Submit an Adverse Event Report

Brand Name
SHWR COMMODE 23 IN TIRES 16 IN W 9153640950
Type of Device
ADAPTOR, HYGIENE
Manufacturer (Section D)
JIANGSU YUYUE MEDICAL EQUIPMENT & SUPPLY CO., LTD
yunyang industrial park
danyang city
jiangsu pro
CH 
MDR Report Key4449638
MDR Text Key5381541
Report Number1531186-2015-00538
Device Sequence Number1
Product Code ILS
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 01/23/2015,01/16/2015
1 Device was Involved in the Event
1 Patient was Involved in the Event
Date FDA Received01/26/2015
Is this an Adverse Event Report? No
Is this a Product Problem Report? Yes
Device Operator Lay User/Patient
Device Model Number6795
Was Device Available for Evaluation? No
Is the Reporter a Health Professional? No
Was the Report Sent to FDA? Yes
Date Report Sent to FDA01/23/2015
Distributor Facility Aware Date01/16/2015
Device Age1 YR
Date Report to Manufacturer01/23/2015
Is This a Reprocessed and Reused Single-Use Device? No
Patient Sequence Number1
Patient Outcome(s) Other;
-
-