International safety notice
Technical Name: Bipolar Modular System for Partial Arthroplasty
Brazil / Anvisa · BRA · Nov 29, 2013
Key facts
| Title | Technical Name: Bipolar Modular System for Partial Arthroplasty |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | - Commercial name: Total Hip Prosthesis ** - Registration: 80062900002 ** - Risk Class: III - HIGH RISK ** - Registration Validity: 2/21/2017 ** - Model: Muller Femoral Stem, C28 Cone Interchangeable Head Protek and Bipolar Head ** - Product Presentation: Sterile packaging containing 01 Total Hip Prosthesis composed of Bipolar Head, Interchangeable Head and Femoral Stem |
| Manufacturer | ORTOBIO IND E COM DE PRODUTOS ORTOPEDICOS LTDA CNPJ03974404000174 ENDEREÇO AVENIDA MAUÁ 1133 ZONA 3 MARINGÁPR TELEFONE4432695045 |
| Models | 80062900002 |
| Date | Nov 29, 2013 |
| Regulator page | anvisa.gov.br |
At a glance
- No Recall
- No Field safety notice
- 100–999 Matching device models in FDA data
- 100–999 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