International safety notice
Commercial Name: Desensibilize Nano-P - Registration Number: 80172310042 - Technical Name: Subst.P/Treatment Dentin Hypersensitivity - Risk class: II - MEDIUM RISK
Brazil / Anvisa · BRA · Sep 16, 2014
Key facts
| Title | Commercial Name: Desensibilize Nano-P - Registration Number: 80172310042 - Technical Name: Subst.P/Treatment Dentin Hypersensitivity - Risk class: II - MEDIUM RISK |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Commercial Name: Desensibilize Nano-P - Registration Number: 80172310042 - Technical Name: Subst.P/Treatment Dentin Hypersensitivity - Risk class: II - MEDIUM RISK - Affected lots: 100415; |
| Manufacturer | FABRICANTE DENTSCARE LTDA CNPJ 05106945000106 AVENIDA EDGAR NELSON MEISTER 474 JOINVILLESC |
| Models | 80172310042, 100415, 040215 |
| Date | Sep 16, 2014 |
| Regulator page | anvisa.gov.br |
At a glance
- No Recall
- No Field safety notice
- 1–9 Matching device models in FDA data
- 1–9 Matching catalog numbers in FDA data
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About International device safety notices
Field safety notices, recalls and safety alerts published by about 30 national medical device regulators outside the United States, matched by Orca1 to FDA device data.
Source: National medical device regulators (as listed), compiled by Orca1