International safety notice
Equipment
Brazil / Anvisa · BRA · Dec 16, 2014
Key facts
| Title | Equipment |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Enteral Nutrition Equipment for use with Macrodrops Infusion Pump, Risk Class II, Brand: Baxter, Registration: 80145240369. Serial numbers: SEE ANNEX - DISTRIBUTION LIST |
| Manufacturer | DETENTOR DO REGISTRO NO BRASIL BAXTER HOSPITALAR LTDA CNPJ 49351786000180 ENDEREÇO RUA HENRI DUBNANT 1383 TORRE B 12ºANDAR CINJ 1201 E 1204 SÃO PAULO SÃO PAULO TELEFONE 1156948497 FABRICANTE BAXTER HEALTHCARE SA SINGAPURE BRANCH ENDEREÇO 2WOODLANDS INDUSTRIAL PARK D CINGAPURE |
| Models | 80145240369 |
| Date | Dec 16, 2014 |
| 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