International safety notice
Updated Alert 2590 (Technosurveillance) - GE Healthcare do Brasil, Com. and Serv.
Brazil / Anvisa · BRA · Jun 22, 2018
Key facts
| Title | Updated Alert 2590 (Technosurveillance) - GE Healthcare do Brasil, Com. and Serv. |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Trade Name: Patient Monitor; Technical Name: Vital Signs Monitor. Product type: Equipment. Risk Class: III. Affected serial numbers: Available in the attached Updated Brazil Installed Base document. Access the full content of Alert 2590 with the respective annexes on the ANVISA Portal (http://portal.anvisa.gov.br/alertas). |
| Manufacturer | EMPRESA DETENTORA DO REGISTRO GE HEALTHCARE DO BRASIL COM E SERV PARA EQUIPAMENTOS MÉDICOHOSPITALARES LTDA CNPJ 00029372000140 AV MAGALHÃES DE CASTRO Nº 4800 11º ANDAR CIDADE JARDIM SÃO PAULO SP TEL 11 30678436 EMAIL TECNOVIGILANGIABRGECOM FABRICANTE DO PRODUTO GE HEALTHCARE FINLAND OY KUORTANEENKATU 2 VALLILA HELSINKI FINLÂNDIA |
| Models | 80071260166, 80071260167 |
| Date | Jun 22, 2018 |
| Regulator page | anvisa.gov.br |
At a glance
- No Recall
- No Field safety notice
- 1–9 Matching device models 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