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

MAUDE Adverse Event Report: TRUMPF MEDIZIN SYSTEME GMBH + CO. KG. TRUMPF TRUSYSTEM 7000DV; TABLE, SURGICAL WITH ORTHOPEDIC ACCESSORIES, AC-POWERED

  • 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
 

TRUMPF MEDIZIN SYSTEME GMBH + CO. KG. TRUMPF TRUSYSTEM 7000DV; TABLE, SURGICAL WITH ORTHOPEDIC ACCESSORIES, AC-POWERED Back to Search Results
Model Number 7000DV
Device Problem Protective Measures Problem (3015)
Patient Problem No Clinical Signs, Symptoms or Conditions (4582)
Event Date 11/20/2021
Event Type  Injury  
Event Description
Patient was positioned on a surgical table and sedated.Table angle was adjusted, and during adjustment the patient's upper body slid off the table.It was determined that the pad underneath the patient was not properly secured to the table, which allowed it to slide during adjustment.No patient injury occurred.Fda safety report id # (b)(4).
 
Search Alerts/Recalls

  New Search  |  Submit an Adverse Event Report

Brand Name
TRUMPF TRUSYSTEM 7000DV
Type of Device
TABLE, SURGICAL WITH ORTHOPEDIC ACCESSORIES, AC-POWERED
Manufacturer (Section D)
TRUMPF MEDIZIN SYSTEME GMBH + CO. KG.
MDR Report Key13534513
MDR Text Key285645533
Report NumberMW5107421
Device Sequence Number1
Product Code JEA
Combination Product (y/n)N
Reporter Country CodeUS
Number of Events Reported1
Summary Report (Y/N)N
Report Source Voluntary
Reporter Occupation Risk Manager
Type of Report Initial
Report Date 02/09/2022
1 Device was Involved in the Event
1 Patient was Involved in the Event
Is this an Adverse Event Report? Yes
Is this a Product Problem Report? Yes
Device Operator Health Professional
Device Model Number7000DV
Was Device Available for Evaluation? Yes
Is the Reporter a Health Professional? No
Initial Date Manufacturer Received Not provided
Initial Date FDA Received02/15/2022
Is This a Reprocessed and Reused Single-Use Device? No
Patient Sequence Number1
Patient Age71 YR
Patient SexFemale
Patient EthnicityNon Hispanic
Patient RaceWhite
-
-