International safety notice
Alert 2488 (Technosurveillance) - Maquet - Patient Ceiling Lifts - Disconnection of the bar in relation to the quick connection ladder
Brazil / Anvisa · BRA · Feb 23, 2018
Key facts
| Title | Alert 2488 (Technosurveillance) - Maquet - Patient Ceiling Lifts - Disconnection of the bar in relation to the quick connection ladder |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Trade name: Patient Ceiling Lifts Technical name: Patient Movement/Transfer Device ANVISA registration number: 80259110133 Risk class: I Affected model: Maxi Sky 2 Affected serial number: 300174590 |
| Manufacturer | EMPRESA DETENTORA DO REGISTRO MAQUET DO BRASIL EQUIPAMENTOS MEDICOS LTDA CNPJ 06028137000130 RUA TENENTE ALBERTO SPICCIATI 200 SÃO PAULO SP FABRICANTE ARJOHUNTLEIGH AB HANS MICHELSENSGATAN 10 211 20 MALMOSUÉCIA TELEFONE 48 61 664 5444 EMAIL KAMILURBANIAKARJOCOM |
| Models | 80259110133, 300174590 |
| Date | Feb 23, 2018 |
| 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