International safety notice
Software
Brazil / Anvisa · BRA · Apr 21, 2015
Key facts
| Title | Software |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | SOFTWARE CENTRICITY PACS IW/ WITH UNIVERSAL VIEWER, Risk Class II, Registration: 80071260309, Centricity PACS-WS in Versions: 3.7.1.1 // 3.7.1.4 // 3.7.2.3 // 3.7.3.1 // 3.7.3.3 // 3.7.3.4 // 3.7.3.5 // 3.7.3.6 // 3.7.3.7 // 3.7.3.8 // 3.7.3.9 // 3.7.3.9 Sp |
| Manufacturer | DETENTOR DO REGISTRO GE HEALTHCARE DO BRASIL CNPJ 00 029 372 0001 40 ENDEREÇO AV MAGALHÃES DE CASTRO Nº 4800 13º ANDAR CIDADE JARDIM SÃO PAULO FABRICANTE GE HEALTHCARE ENDEREÇO 540 W NORTHWEST HIGHWAY BARRINGTON IL 60010 ESTADOS UNIDOS |
| Models | 3.7.1.4, 3.7.3.5, 3.7.3.9, 80071260309, 3.7.3.3, 3.7.3.4, 3.7.3.8, 3.7.3.6, 3.7.1.1, 3.7.2.3, 3.7.3.1, 3.7.3.7 |
| Date | Apr 21, 2015 |
| 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