International safety notice
Technical name: Infusion Pump
Brazil / Anvisa · BRA · Nov 16, 2017
Key facts
| Title | Technical name: Infusion Pump |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Trade name: Infusion Pump Technical name: Infusion Pump ANVISA registration number: 80113010024 Risk class: III Affected model: GH Infusion Pump /PK Infusion Pump Affected serial numbers: pumps manufactured before September/2008 - attached list. |
| Manufacturer | EMPRESA DETENTORA DO REGISTRO RESPIRATORY CARE HOSPITALAR LTDA CNPJ 02126465000119 RUA PADRE ABES 118 CENTRO JUQUITIBA SP FABRICANTE CAREFUSION SWITZERLAND 317 SARL SUÉCIA |
| Models | 80113010024 |
| Date | Nov 16, 2017 |
| Regulator page | anvisa.gov.br |
At a glance
- No Recall
- No Field safety notice
- 1–9 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