International safety notice
Portable Pulse Oximeter Model M1000
Brazil / Anvisa · BRA · Jan 18, 2016
Key facts
| Title | Portable Pulse Oximeter Model M1000 |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | M1000 Pulse Oximeter; |
| Manufacturer | J G MORIYA REPRESENTAÇÃO IMPORTADORA EXPORTADORA E COMERCIAL LTDA CNPJ 67882621000117 ENDEREÇO RUA COLORADO 279 VILA CARIOCA SÃO PAULO SP CEP 04225050 TEL 55 11 29149352 E F 55 11 29141943 |
| Models | 13400370, 13400353, 13400351, 13400365, 13400349, 13400369, 13400344, 13400343, 13400340, 13400352, 13400367, 13400347 and 24 more |
| Date | Jan 18, 2016 |
| Regulator page | anvisa.gov.br |
At a glance
- No Recall
- No Field safety notice
- 1–9 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