International safety notice
Technical name: Limb Compression System
Brazil / Anvisa · BRA · Jun 26, 2017
Key facts
| Title | Technical name: Limb Compression System |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Commercial name: Flowtron ACS900 System Technical name: Limb Compression System ANVISA registration number: 80259110105 Risk class: I Affected model: Flowtron ACS900 System Affected serial numbers: All Serial Numbers/All Batches manufactured between 09/26 /2014 and 12/20/2016, with software V1.099. |
| Manufacturer | EMPRESA DETENTORA DO REGISTRO MAQUET DO BRASIL EQUIPAMENTOS MEDICOS LTDA 06028137000130 RUA TENENTE ALBERTO SPICCIATI 200 SÃO PAULOSP 11 26087426 ARJOHUNTLEIGH AB SUÉCIA HANS MICHELSENSGATAN 10 MALMO 48698663136 FABRICANTE MAQUET DO BRASIL EQUIPAMENTOS MEDICOS LTDA 06028137000130 RUA TENENTE ALBERTO SPICCIATI 200 SÃO PAULOSP 11 26087426 ARJOHUNTLEIGH AB SUÉCIA HANS MICHELSENSGATAN 10 MALMO 48698663136 |
| Models | ACS900, V1.099, 80259110105 |
| Date | Jun 26, 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