International safety notice

Alert 2954 (Technovigilance) - Varian Medical Systems Brasil Ltda - Acuity IX Need to update the equipment's SSL certificate.

Brazil / Anvisa · BRA · Aug 16, 2019

Key facts

Title Alert 2954 (Technovigilance) - Varian Medical Systems Brasil Ltda - Acuity IX Need to update the equipment's SSL certificate.
Regulator Brazil / Anvisa
Country BRA
Brand Nome Comercial: Acuity IX Technical Name: Radiotherapy Simulator ANVISA registration number: 10405410018 Risk Class: III Affected model: N/A Affected serial numbers: H770531
Manufacturer EMPRESA DETENTORA DO REGISTRO VARIAN MEDICAL SYSTEMS BRASIL LTDA CNPJ 03009915000156 RUA SÃO CARLOS DO PINHAL 696 9 ANDAR SÃO PAULO SP TEL 1134572655 EMAIL FERNANDOMESQUITAVARIANCOM FABRICANTE DO PRODUTO VARIAN MEDICAL SYSTEMS INC 911 HANSEN WAY PALO ALTO CA ESTADOS UNIDOS
Models H770531, 10405410018
Date Aug 16, 2019
Regulator page anvisa.gov.br

At a glance

  • No Recall
  • No Field safety notice
  • 100–999 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

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