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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: NOBEL BIOCARE AB REPLACE SELECT TAPERED PMC 6.0 6X11.5MM; ENDOSSEOUS DENTAL IMPLANT

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NOBEL BIOCARE AB REPLACE SELECT TAPERED PMC 6.0 6X11.5MM; ENDOSSEOUS DENTAL IMPLANT Back to Search Results
Model Number 37317
Medical Device Problem Code Loss of Osseointegration (2408)
Health Effect - Clinical Code Failure of Implant (1924)
Date of Event 06/20/2022
Type of Reportable Event Serious Injury
Event or Problem Description
Implant failed due to a loss of osseointegration.
 
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Brand Name
REPLACE SELECT TAPERED PMC 6.0 6X11.5MM
Common Device Name
ENDOSSEOUS DENTAL IMPLANT
Manufacturer (Section D)
NOBEL BIOCARE AB
dimbovägen 2
karlskoga 69151
SW  69151
MDR Report Key15006515
Report Number2027971-2022-089949
Device Sequence Number19436574
Product Code DZE
UDI-Device Identifier07332747073324
UDI-Public(01)07332747073324(10)12106109(17)230210
Combination Product (Y/N)N
Initial Reporter CountryCA
Number of Events Summarized1
Summary Report (Y/N)N
Device Implanted Year2019
Device Explanted Year2022
Serviced by Third Party (Y/N)N
Reporter Type Importer
Initial Reporter Occupation Dentist
Type of Report Initial
Report Date (Section F) 07/13/2022
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? No
Operator of Device Health Professional
Device Expiration Date02/10/2023
Device Model Number37317
Device Catalogue Number37317
Device Lot Number12106109
Was Device Available for Evaluation? No
Is the Reporter a Health Professional? Yes
Was the Report Sent to FDA? No
Distributor Facility Aware Date07/11/2022
Event Location Outpatient Treatment Facility
Initial Date Received by Manufacturer Not provided
Initial Report FDA Received Date07/13/2022
Is This a Single-Use Device that was
Reprocessed and Reused on a Patient? (Y/N)
No
Usage of Device A
Patient Sequence Number1
Outcome Attributed to Adverse Event Required Intervention;
Patient Age77 YR
Patient SexFemale
Date Report Sent to FDA07/13/2022
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