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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: NOBEL BIOCARE AB REPLACE SELECT TAPERED PMC RP 4.3X16MM; ENDOSSEOUS DENTAL IMPLANT

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NOBEL BIOCARE AB REPLACE SELECT TAPERED PMC RP 4.3X16MM; ENDOSSEOUS DENTAL IMPLANT Back to Search Results
Model Number 37309
Medical Device Problem Code Loss of Osseointegration (2408)
Health Effect - Clinical Code Failure of Implant (1924)
Date of Event 10/03/2022
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 RP 4.3X16MM
Common Device Name
ENDOSSEOUS DENTAL IMPLANT
Manufacturer (Section D)
NOBEL BIOCARE AB
dimbovägen 2
karlskoga 69151
SW  69151
MDR Report Key15653905
Report Number2027971-2022-123973
Device Sequence Number5966780
Product Code DZE
UDI-Device Identifier07332747073409
UDI-Public(01)07332747073409(10)12066468(17)210501
Combination Product (Y/N)N
Initial Reporter CountryRS
Number of Events Summarized1
Summary Report (Y/N)N
Device Implanted Year2020
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) 10/21/2022
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 Date05/01/2021
Device Model Number37309
Device Catalogue Number37309
Device Lot Number12066468
Was Device Available for Evaluation? No
Is the Reporter a Health Professional? Yes
Was the Report Sent to FDA? No
Distributor Facility Aware Date10/19/2022
Event Location Outpatient Treatment Facility
Initial Date Received by Manufacturer Not provided
Initial Report FDA Received Date10/21/2022
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 Age69 YR
Patient SexFemale
Date Report Sent to FDA10/21/2022
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