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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: SIRONA DENTAL SYSTEMS GMBH MIDWEST TRADITION HANDPIECE; HANDPIECE, AIR-POWERED, DENTAL PRODUCT CODE EFB

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SIRONA DENTAL SYSTEMS GMBH MIDWEST TRADITION HANDPIECE; HANDPIECE, AIR-POWERED, DENTAL PRODUCT CODE EFB Back to Search Results
Catalog Number 790044
Device Problem Detachment of Device or Device Component (2907)
Patient Problem No Clinical Signs, Symptoms or Conditions (4582)
Event Type  malfunction  
Manufacturer Narrative
1 of 1 devices were returned for evaluation.Evaluation of 1 device found normal chuck wear and the turbine needed to be replaced.The device was repaired and returned to the customer.This event is being submitted as part of vmsr.Only one event was received for this device during this quarter.
 
Event Description
This report summarizes malfunction event where a midwest tradition handpiece would not hold burs.No injury resulted.
 
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Brand Name
MIDWEST TRADITION HANDPIECE
Type of Device
HANDPIECE, AIR-POWERED, DENTAL PRODUCT CODE EFB
Manufacturer (Section D)
SIRONA DENTAL SYSTEMS GMBH
fabrikstrasse 31
bensheim, hessen D-646 25
GM  D-64625
Manufacturer (Section G)
SIRONA DENTAL SYSTEMS GMBH
fabrikstrasse 31
bensheim, hessen D-646 25
GM   D-64625
Manufacturer Contact
hannah seevaratnam
221 w. philadelphia st.
york, PA 17401
7178494593
MDR Report Key16789744
MDR Text Key313764809
Report Number9614977-2023-00012
Device Sequence Number1
Product Code EFB
Combination Product (y/n)N
PMA/PMN Number
K131319
Number of Events Reported1
Summary Report (Y/N)Y
Report Source Manufacturer
Reporter Occupation Other
Type of Report Initial
Report Date 04/21/2023
1 Device was Involved in the Event
1 Patient was Involved in the Event
Date FDA Received04/21/2023
Is this an Adverse Event Report? No
Is this a Product Problem Report? No
Device Catalogue Number790044
Patient Sequence Number1
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