International safety notice
Technical name: Scintigraphic Camera (Gama Camara)
Brazil / Anvisa · BRA · Oct 25, 2016
Key facts
| Title | Technical name: Scintigraphic Camera (Gama Camara) |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Two products are affected by Campo's action: 1. Commercial name: E.CAM SIGNATURE SERIES BRAND SIEMENS Technical name: Camara Cintilografica (Gama Camara) Registration 10234230040 Model: E.CAM Signature Series, brand SIEMENS /// 2. Commercial name: SPECT SYSTEM Registration 10345161991 Model: Symbia E - Technical name: Nuclear Image Formation System - ANVISA registration number: 80004040126 /// Affected series numbers: 3002; |
| Manufacturer | EMPRESA DETENTORA DO REGISTRO SIEMENS HEALTHCARE DIAGNÓSTICOS SA CNPJ 01449930000190 AV MUTINGA 3800 7º ANDAR PIRITUBA SÃO PAULOSP 11 39083877 CAROLINEHAYASHIDASIEMENSCOM FABRICANTE SIEMENS MEDICAL SOLUTIONS USA INC 2501 N BARRINGTON ROAD HOFFMAN ESTATES ILLINOIS 60192 ESTADOS UNIDOS |
| Models | 80004040126, 11048, 10345161991, 11194, 11073, 10234230040, 11463, 10012 |
| Date | Oct 25, 2016 |
| Regulator page | anvisa.gov.br |
At a glance
- No Recall
- No Field safety notice
- 1–9 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