International safety notice
Lung Ventilator - E360E/E360P/E360S/E360T/E360T+ - Registration with Anvisa No. 80113010025 - Risk Class III
Brazil / Anvisa · BRA · Jul 2, 2014
Key facts
| Title | Lung Ventilator - E360E/E360P/E360S/E360T/E360T+ - Registration with Anvisa No. 80113010025 - Risk Class III |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Lung Ventilator - E360E/E360P/E360S/E360T/E360T+ - Registration with Anvisa No. 80113010025 - Risk Class III ## Series affected: See Distribution Map in Annex 1 |
| Manufacturer | EMPRESA DETENTORA DO REGISTRO NO BRASIL RESPIRATORY CARE HOSPITALAR LTDA CNPJ 02126465000119 RUA PADUR ALVES Nº 118 JUQUITIBASP FABRICANTE NEWPORT MEDICAL INSTRUMENTS 1620 SUNFLOWER AVENUE COSTA MESA CA 92626 |
| Models | 80113010025, E360P, E360T, E360E, E360S |
| Date | Jul 2, 2014 |
| Regulator page | anvisa.gov.br |
At a glance
- No Recall
- No Field safety notice
- 10–99 Matching device models in FDA data
- 10–99 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