International safety notice
Osteo-articular implants - Various
Brazil / Anvisa · BRA · Jan 23, 2013
Key facts
| Title | Osteo-articular implants - Various |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | REG.10395270003-PROD.:Acetabulum of Charnley Incomepe REG.10395270005-PROD.:Charnley Incomepe Total Hip Prosthesis REG.10395270006-PROD.:Thompson Incomepe Type Partial Hip Prosthesis REG.10395270008-PROD.:Incomepe Shoulder Prosthesis REG.10395270012-PROD.: Muller Incomepe Acetabulum REG.10395270017-PROD.:Incomepe Interchangeable Head REG.10395270022-PROD.: Incomepe Bipolar Acetabulum REG.10395270023-PROD.: Incomepe Glenoid Component REG.10395270026-PROD.:Neer II Incomepe Interchangeable Head REG.10395270042-PROD.:SINJ Knee Prosthesis |
| Manufacturer | INCOMEPE INDÚSTRIA DE MATERIAIS CIRURGICOS LTDA CNPJ 57212870000141 RUA UM Nº 35 BARRO BRANCO COTIA |
| Models | REG.10395270008-PROD, REG.10395270003-PROD, REG.10395270023-PROD, REG.10395270006-PROD, REG.10395270026-PROD, REG.10395270005-PROD, REG.10395270012-PROD, REG.10395270017-PROD, REG.10395270042-PROD, REG.10395270022-PROD |
| Date | Jan 23, 2013 |
| Regulator page | anvisa.gov.br |
At a glance
- No Recall
- No Field safety notice
- 1–9 Matching device models 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