International safety notice
Technical name: Equipment for Sample Preparation for In Vitro Diagnostics
Brazil / Anvisa · BRA · May 22, 2017
Key facts
| Title | Technical name: Equipment for Sample Preparation for In Vitro Diagnostics |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Trade name: Abbott VP2000 Processor Technical name: Equipment for Sample Preparation for In Vitro Diagnostics ANVISA registration number: 80146509035 Risk class: I Affected model: Not applicable Affected serial numbers: 36001 |
| 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 MOLECULAR INC ENDEREÇO DES PLAINES IL 60018 USA IOSENSE WEBSTER INC 3333 DIAMOND CANYON RD DIAMOND BAR CA 91765 EUA |
| Models | VP2000, 80146509035, 36001 |
| Date | May 22, 2017 |
| Regulator page | anvisa.gov.br |
At a glance
- No Recall
- No Field safety notice
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