International safety notice
Software
Brazil / Anvisa · BRA · Aug 15, 2017
Key facts
| Title | Software |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Trade name: TrueBeam, VitalBeam and Edge Technical name: ANVISA registration number: 10405410022 Risk class: III Affected model: N/A Affected serial numbers: H192524, H191578, H191700, H192523, H191762, H191581, H191559, H192534 |
| Manufacturer | EMPRESA DETENTORA DO REGISTRO VARIAN MEDICAL SYSTEMS BRASIL LTDA CNPJ 03009915000156 RUA SÃO CARLOS DO PINHAL 696 7 E 9 ANDAR SÃO PAULO SP FABRICANTE VARIAN MEDICAL SYSTEMS INC 911 HANSEN WAY PALO ALTO CA ALEMANHA TELEFONE 1 650 424 5700 EMAIL PETECORONADOVARIANCOM |
| Models | H191762, H191559, H192524, H191581, 10405410022, H191578, H192523, H191700, H192534 |
| Date | Aug 15, 2017 |
| 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