International safety notice
Alert 2824 (Technovigilance) Tecmedic Comércio de Produtos Médicos Ltda Aspirex S Possibility of failure in the labeling of specific batch units.
Brazil / Anvisa · BRA · Mar 20, 2019
Key facts
| Title | Alert 2824 (Technovigilance) Tecmedic Comércio de Produtos Médicos Ltda Aspirex S Possibility of failure in the labeling of specific batch units. |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Trade Name: Aspirex S Technical Name: Catheters ANVISA registration number: 80202910072 Risk Class: II Affected model: 80232 Affected serial numbers: 190114 |
| Manufacturer | EMPRESA DETENTORA DO REGISTRO TECMEDIC COMÉRCIO DE PRODUTOS MÉDICOS LTDA CNPJ 05638301000169 RUA BRASILIO CUMAN 566 SÃO BRÁZ CURITIBA PARANÁ TEL 41 32337887 EMAIL REGULATORIOCONTECSERVCOMBR FABRICANTE DO PRODUTO STRAUB MEDICAL AG STRAUBSTRASSE 12 7323 WANGS SUÍÇA |
| Models | 80202910072, 190114, 80232 |
| Date | Mar 20, 2019 |
| 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