International safety notice
Technical name: EQUIPMENT FOR PREPARING SAMPLES FOR IN VITRO DIAGNOSIS
Brazil / Anvisa · BRA · Jun 16, 2016
Key facts
| Title | Technical name: EQUIPMENT FOR PREPARING SAMPLES FOR IN VITRO DIAGNOSIS |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Trade name: APTIO AUTOMATION ANVISA registration number: 10345161904 Risk class: I Affected serial numbers: APT.0154.12.14 ; |
| 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 HEALTHCARE DIAGNOSTICS INC 511 BENEDICT AVENUE TARRYTOWN NEW YORK 10591 |
| Models | APT.0133.09.14, APT.0179.02.15, APT.0209.04.15, APT.0266.10.15, APT.0154.12.14, 10345161904 |
| Date | Jun 16, 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