MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a health professional report with the FDA on 2020-03-31 for NOBELREPLACE CC RP 4.3X13MM 36708 manufactured by Nobel Biocare Usa Inc.
[185886024]
Implant failed due to failure to osseointegrate.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 2027971-2020-08882 |
MDR Report Key | 9907584 |
Report Source | HEALTH PROFESSIONAL |
Date Received | 2020-03-31 |
Date of Event | 2020-03-17 |
Device Manufacturer Date | 2019-12-02 |
Date Added to Maude | 2020-03-31 |
Event Key | 0 |
Report Source Code | Manufacturer report |
Manufacturer Link | Y |
Number of Patients in Event | 0 |
Adverse Event Flag | 3 |
Product Problem Flag | 3 |
Reprocessed and Reused Flag | 3 |
Reporter Occupation | DENTIST |
Health Professional | 3 |
Initial Report to FDA | 3 |
Report to FDA | 3 |
Event Location | 3 |
Manufacturer Contact | WILLEM VAN ALST |
Manufacturer Street | KOZAKKENBERG 4 |
Manufacturer City | BELFELD 5951DL |
Manufacturer Country | NL |
Manufacturer Postal | 5951 DL |
Manufacturer Phone | 683284947 |
Manufacturer G1 | NOBEL BIOCARE USA INC |
Manufacturer Street | 22725 SAVI RANCH |
Manufacturer City | YORBA LINDA CA 928874609 |
Manufacturer Country | US |
Manufacturer Postal Code | 928874609 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | NOBELREPLACE CC RP 4.3X13MM |
Generic Name | ENDOSSEOUS DENTAL IMPLANT |
Product Code | DZE |
Date Received | 2020-03-31 |
Catalog Number | 36708 |
Lot Number | 13091808 |
Operator | HEALTH PROFESSIONAL |
Device Availability | N |
Device Eval'ed by Mfgr | R |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | NOBEL BIOCARE USA INC |
Manufacturer Address | 22725 SAVI RANCH YORBA LINDA CA 928874609 US 928874609 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Required No Informationntervention | 2020-03-31 |