International safety notice
Alert 2382 Updated (Technosurveillance) Siemens - ACUSON Diagnostic Ultrasound System Software Update
Brazil / Anvisa · BRA · Sep 25, 2017
Key facts
| Title | Alert 2382 Updated (Technosurveillance) Siemens - ACUSON Diagnostic Ultrasound System Software Update |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Trade name: ACUSON Diagnostic Ultrasound System Technical name: Ultrasound Device ANVISA registration number: 10345162017 Product type: Equipment Risk class: II Affected model: ACUSON S2000 Affected serial numbers (updated list): 211784; Access the full content of Alert 2382 with the respective annexes on the ANVISA Portal (http://portal.anvisa.gov.br/alertas). |
| Manufacturer | EMPRESA DETENTORA DO REGISTRO SIEMENS HEALTHCARE DIAGNÓSTICOS SA CNPJ 01449930000190 AV MUTINGA 3800 4º ANDAR PIRITUBA SP FABRICANTE SIEMENS MEDICAL SOLUTIONS USA INC 685 EAST MIDDLEFIELD ROAD MOUNTAIN VIEW CA 94043 |
| Models | 213596, 215426, 213886, 214179, 214525, 10345162017, 211771, 211784, 215421, 215936, 211397, 215419 and 17 more |
| Date | Sep 25, 2017 |
| 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