International safety notice
DEFIBRILLATOR
Brazil / Anvisa · BRA · May 17, 2010
Key facts
| Title | DEFIBRILLATOR |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | LIFEPACK 12 MONITORING AND DEFIBRILLATION SYSTEM - LIFEPACK 20 DEFIBRILLATOR AND LIFEPACK 9P MONITORING AND DEFIBRILLATION SYSTEM - Registered with ANVISA under numbers 10339190080 - 10339191171 and 10339190082 - respectively. |
| Manufacturer | DETENTOR DO REGISTRO DO PRODUTO NO BRASIL MEDTRONIC COMERCIAL |
| Models | 10339190082, A3o.pdf?MOD=AJPERES, 10339190080, 10339191171, 8c374d80428449fd9e2aff01cce3dc94 |
| Date | May 17, 2010 |
| Regulator page | anvisa.gov.br |
At a glance
- No Recall
- No Field safety notice
- 1–9 Matching device models in FDA data
- 1–9 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