FDA Adverse Event Injury Summary report: N

NOBELREPLACE CC TIULTRA NP 3.5X11.5MM

MDR report key: 13969666 · Received March 31, 2022

Report

Report Number
2027971-2022-056347
Event Type
Injury
Date Received
March 31, 2022
Date of Event
March 17, 2022
Report Date
March 31, 2022
Manufacturer
NOBEL BIOCARE AB
Product Code
DZE
UDI-DI
07332747128307
Adverse Event
Yes
Report Source
Distributor report
Reporter Location
US
Reporter Occupation
DENTIST
Health Professional
Yes

Narratives

Description of Event or Problem · 0

IMPLANT FAILED DUE TO AN OSSEOINTEGRATION PROBLEM. (B)(6) 2022 08:20:04 CET ((B)(6)) PHONE (B)(6) MUST BE IMPLANT FAILED DUE TO A FAILURE TO OSSEOINTEGRATE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1105457 NOBELREPLACE CC TIULTRA NP 3.5X11.5MM ENDOSSEOUS DENTAL IMPLANT DZE NOBEL BIOCARE AB 300339 12192048 07332747128307

Patients

Seq Age Sex Outcome Treatment
1 63 YR Female Required Intervention