International safety notice
Technical name: Positron Emission Tomography Equipment
Brazil / Anvisa · BRA · Jan 11, 2017
Key facts
| Title | Technical name: Positron Emission Tomography Equipment |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Trade name: Positron Emission Tomography Equipment Technical name: Positron Emission Tomography Equipment ANVISA registration number: 10345162013 Risk class: III Affected model: Biograph mCT / Biohgraph mCT Flow Affected serial numbers: 1010;11045;11046 ;11072 and 11036 |
| Manufacturer | EMPRESA DETENTORA DO REGISTRO SIEMENS HEALTHCARE DIAGNÓSTICOS SA CNPJ 01449930000190 ENDEREÇO AV MUTINGA 3800 7º ANDAR PIRITUBA SÃO PAULOSP TELEFONE 0800 129 633 FABRICANTE SIEMENS MEDICAL SOLUTION SA 810 INNOVATION DRIVE KNOXVILLE TN 37932 ESTADOS UNIDOS |
| Models | 10345162013, 11046, 11072, 11045, 11036 |
| Date | Jan 11, 2017 |
| 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