International safety notice
Technical name: DEFIBRILLATOR /MONITOR
Brazil / Anvisa · BRA · Feb 7, 2017
Key facts
| Title | Technical name: DEFIBRILLATOR /MONITOR |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Commercial name: Defibrillator/Monitor Technical name: DEFIBRILLATOR/MONITOR ANVISA registration number: 80102511541 Risk class: III Affected model: LIFEPAK 15 Affected serial numbers: 44574467; |
| Manufacturer | EMPRESA DETENTORA DO REGISTRO VR MEDICAL LTDA ENDEREÇO RUA BATATAES 391 CONJS 11 13 E 8º ANDAR SP TELEFONES DE CONTATO 11 3885 76 33 RAMAL 105 FABRICANTE PHYSIOCONTROL INC 11811 WILLOWS ROAD NE REDMOND WA 98052 EUA |
| Models | 80102511541, 44574771, 44574467, 44574821 |
| Date | Feb 7, 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