International safety notice
Alert 2485 (Technosurveillance) - Siemens - Artis One Angiography Equipment Potential fall of part of the equipment
Brazil / Anvisa · BRA · Feb 22, 2018
Key facts
| Title | Alert 2485 (Technosurveillance) - Siemens - Artis One Angiography Equipment Potential fall of part of the equipment |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Trade name: Artis One Angiography Equipment Technical name: Angiography Equipment ANVISA registration number: 10345162020 Risk class: III Affected model: Artis One Affected serial number: 82190; |
| Manufacturer | EMPRESA DETENTORA DO REGISTRO SIEMENS HEALTHCARE DIAGNÓSTICOS LTDA CNPJ 01449930000190 AV MUTINGA 3800 4º E 5º ANDAR PIRITUBA SÃO PAULO FABRICANTE SIEMENS SHENZHEN MAGNETIC RESSONANCE LTDSSMR GAOXIN C AVENUE 2ND HITECH INDUSTRIAL PARK SHENZHEN GUANGDONG 518057 CHINA |
| Models | 82090, 82032, 82161, 82063, 82190, 82136, 82176, 82046, 82110, 82170, 82030, 82216 and 12 more |
| Date | Feb 22, 2018 |
| Regulator page | anvisa.gov.br |
At a glance
- No Recall
- No Field safety notice
- 10–99 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