International safety notice
Technical name: HEMATOLOGIC ANALYZER
Brazil / Anvisa · BRA · Mar 2, 2017
Key facts
| Title | Technical name: HEMATOLOGIC ANALYZER |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Trade name: CELL-DYN RUBY Technical name: HEMATOLOGIC ANALYZER ANVISA registration number: 80146501507 Risk class: II Affected model: Not applicable Affected serial numbers: 70002BG; |
| Manufacturer | EMPRESA DETENTORA DO REGISTRO ABBOTT LABORATÓRIOS DO BRASIL CNPJ 56998701000116 ENDEREÇO RUA MICHIGAN 735 CIDADE MONÇÕES SÃO PAULO SP CEP 04566905 CONTATO 55 11 5536 7246 FAX 55 11 5536 7062 FABRICANTE ABBOTT LABORATORIES ENDEREÇO 100 ABBOTT PARK ROAD ABBOTT PARK ILLINOIS 60064 |
| Models | 70067BG, 70038BG, 70028BG, 70056BG, 70044BG, 70072BG, 70114BG, 70134BG, 70167BG, 70100BG, 70063BG, 70086BG and 105 more |
| Date | Mar 2, 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