International safety notice
Technical name: Modular System for Total Arthroplasty
Brazil / Anvisa · BRA · Oct 22, 2016
Key facts
| Title | Technical name: Modular System for Total Arthroplasty |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Commercial name: System for Hip Arthroplasty Hybrid Technical name: Modular System for Total Arthroplasty ANVISA registration number: 10417940085 Risk class: III Affected model: PHENOM Poly Acetabular Insert (04.13.13.xxxxx) / PHENOM Poly Acetabular Insert Posterior Roof (04.13.14.xxxxx) |
| Manufacturer | EMPRESA DETENTORA DO REGISTRO MDT INDUSTRIA COMÉRCIO IMPORTAÇÃO E EXPORTAÇÃO DE IMPLANTES SA AVENIDA BRASIL 2983 DISTRITO INDUSTRIAL SP RIO CLARO FABRICANTE MDT INDUSTRIA COMÉRCIO IMPORTAÇÃO E EXPORTAÇÃO DE IMPLANTES SA AVENIDA BRASIL 2983 DISTRITO INDUSTRIAL SP RIO CLARO |
| Models | 04.13.14.xxxxx, 10417940085, 04.13.13.xxxxx |
| Date | Oct 22, 2016 |
| Regulator page | anvisa.gov.br |
At a glance
- No Recall
- No Field safety notice
- 10–99 Matching device models in FDA data
- 10–99 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