International safety notice
Technical name: AUTOMATIC / SEMI-AUTOMATIC EXTERNAL DEFIBRILLATOR
Brazil / Anvisa · BRA · Jan 19, 2017
Key facts
| Title | Technical name: AUTOMATIC / SEMI-AUTOMATIC EXTERNAL DEFIBRILLATOR |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Trade name: Automatic External Defibrillator Registration Technical name: AUTOMATIC / SEMI-AUTOMATIC EXTERNAL DEFIBRILLATOR ANVISA registration number: 80102511545 Risk class: III High Risk Affected model: LIFEPAK 1000 |
| Manufacturer | EMPRESA DETENTORA DO REGISTRO VR MEDICAL LTDA CNPJ 04718143000194 RUA BATATAES 391 CONJS 11 13 E 8º ANDAR SÃO PAULOSP FABRICANTE PHYSIOCONTROL INC 11811 WILLOWS ROAD NE REDMOND WA 98052 ESTADOS UNIDOS |
| Models | 80102511545 |
| Date | Jan 19, 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