International safety notice
Equipment.
Brazil / Anvisa · BRA · May 16, 2012
Key facts
| Title | Equipment. |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | CONTINUUM INFUSION SYSTEM, codes MIK 200A, MIL 200B, 3015153, 3015155, 3015156, 3015157, 3015158, 3015159, 3015160 and 3015161. Anvisa registration no. 80172890011. |
| Manufacturer | DETENTOR DE REGISTRO MEDRAD DO BRASIL DISTRIBUIÇÃO IMPORTAÇÃO EQUIP PROD SÁUDE E SERVIÇOS TÉCNICOS LTDA CNPJ 00506570000158 AV NOVE DE JULHO 5109 11 ANDAR SÃO PAULO SP TEL 11 37026008 FAX 11 30784026 |
| Models | 3015157, 3015158, 3015153, 3015160, 3015156, 80172890011, 3015155, 3015161, 3015159 |
| Date | May 16, 2012 |
| Regulator page | anvisa.gov.br |
At a glance
- No Recall
- No Field safety notice
- 10–99 Matching device models in FDA data
- 1–9 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