International safety notice
Technical name: Patient Lift
Brazil / Anvisa · BRA · Oct 3, 2016
Key facts
| Title | Technical name: Patient Lift |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Trade name: Patient Lift Technical name: Patient Lift ANVISA registration number: 80259110103 Risk class: - Low Risk Affected model: Maximove Affected serial numbers: 300044700; |
| Manufacturer | EMPRESA DETENTORA DO REGISTRO MAQUET DO BRASIL EQUIPAMENTOS MEDICOS LTDA CNPJ 06028137000130 RUA TENENTE ALBERTO SPICCIATI 200 SÃO PAULOSP TELEFONE 11 26087426 EMAIL GIORGIOGENTILEGETINGECOM FABRICANTE ARJOHUNTLEIGH AB HANS MICHELSENSGATAN 10 211 20 MALMÖ SUÉCIA |
| Models | 80259110103, 300072094, 300072093, 300070780-300070791, 300044700, 300050411, 300050413 |
| Date | Oct 3, 2016 |
| 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