International safety notice
Deskart Injet Urethral Probe, Tracheal Aspiration Probe
Brazil / Anvisa · BRA · Dec 18, 2012
Key facts
| Title | Deskart Injet Urethral Probe, Tracheal Aspiration Probe |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Deskart Injet Urethral Probe, registration no. 80074020004, Deskat Injet Tracheal Aspiration Probe, registration no. 80074020005 |
| Manufacturer | DESKART INJET INDUSTRIA CIRURGICA LTDAME CNPJ 72681455000120 ESTABELECIDA NA GIOVANI MORETTI 136 SÃO CAETANO DO SUL |
| Models | 80074020004, 80074020005 |
| Date | Dec 18, 2012 |
| Regulator page | anvisa.gov.br |
At a glance
- No Recall
- No Field safety notice
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