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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: SIRONA DENTAL SYSTEMS GMBH MIDWEST E PLUS 1:5; HANDPIECE, AIR-POWERED, DENTAL

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SIRONA DENTAL SYSTEMS GMBH MIDWEST E PLUS 1:5; HANDPIECE, AIR-POWERED, DENTAL Back to Search Results
Catalog Number 875205
Device Problem Detachment of Device or Device Component (2907)
Patient Problem No Consequences Or Impact To Patient (2199)
Event Type  malfunction  
Manufacturer Narrative
Additional serial numbers included in this report: (b)(4).9 of 10 devices were returned for evaluation.Multiple unsuccessful attempts were made to obtain 1 device.Evaluation of 2 devices found normal chuck wear and the turbines needed to be replaced.The devices were repaired and returned to the customers.Evaluation of 7 devices found chuck wear and lack of maintenance.The devices were cleaned of debris and the turbines were replaced.The devices were repaired and returned to the customers.
 
Event Description
This report summarizes 10 malfunction events.This report summarizes ten malfunction events where a midwest e plus 1:5 handpiece would not hold dental burs.There were no injuries in any of the events.
 
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Brand Name
MIDWEST E PLUS 1:5
Type of Device
HANDPIECE, AIR-POWERED, DENTAL
Manufacturer (Section D)
SIRONA DENTAL SYSTEMS GMBH
fabrikstrasse 31
bensheim, D-646 25
GM  D-64625
Manufacturer (Section G)
SIRONA DENTAL SYSTEMS GMBH
fabrikstrasse 31
bensheim, D-646 25
GM   D-64625
Manufacturer Contact
karl nittinger
221 w. philadelphia st.
suite 60w
york, PA 17401
7178494424
MDR Report Key9262988
MDR Text Key184702663
Report Number9614977-2019-00148
Device Sequence Number1
Product Code EFB
Combination Product (y/n)N
PMA/PMN Number
K972436
Number of Events Reported10
Summary Report (Y/N)Y
Report Source Manufacturer
Type of Report Initial
Report Date 10/31/2019
1 Device was Involved in the Event
1 Patient was Involved in the Event
Date FDA Received10/31/2019
Is this an Adverse Event Report? No
Is this a Product Problem Report? Yes
Device Operator No Information
Device Catalogue Number875205
Type of Device Usage N
Patient Sequence Number1
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