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

MAUDE Adverse Event Report: C.T.M. SHANGHAI MOTORIZED 3-WHEELED VEHICLE FOR OUTSIDE TRANSPORT; 890.3800

  • 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
 

C.T.M. SHANGHAI MOTORIZED 3-WHEELED VEHICLE FOR OUTSIDE TRANSPORT; 890.3800 Back to Search Results
Model Number L-3XB
Device Problem Battery Problem (2885)
Patient Problem No Consequences Or Impact To Patient (2199)
Event Type  No Answer Provided  
Event Description
Per provider; charge batteries over night, shows full charge, when in use the batteries drop to empty and strand the end user.
 
Search Alerts/Recalls

  New Search  |  Submit an Adverse Event Report

Brand Name
MOTORIZED 3-WHEELED VEHICLE FOR OUTSIDE TRANSPORT
Type of Device
890.3800
Manufacturer (Section D)
C.T.M. SHANGHAI
1158 yuan qu road
anting town
shanghai 2018 05
CH  201805
MDR Report Key4201767
MDR Text Key20777304
Report Number1531186-2014-05093
Device Sequence Number1
Product Code INI
Combination Product (y/n)N
Reporter Country CodeCA
Number of Events Reported1
Summary Report (Y/N)N
Report Source Manufacturer
Source Type Invalid Data
Reporter Occupation Medical Equipment Company Technician/Representative
Type of Report Initial
Report Date 10/25/2014,10/03/2014
1 Device was Involved in the Event
1 Patient was Involved in the Event
Date FDA Received10/27/2014
Is this an Adverse Event Report? No
Is this a Product Problem Report? Yes
Device Operator Lay User/Patient
Device Model NumberL-3XB
Was Device Available for Evaluation? No
Is the Reporter a Health Professional? No
Was the Report Sent to FDA? Yes
Date Report Sent to FDA10/25/2014
Distributor Facility Aware Date10/03/2014
Device Age10 MO
Date Report to Manufacturer10/25/2014
Is This a Reprocessed and Reused Single-Use Device? No
Patient Sequence Number1
Patient Outcome(s) Other;
-
-