International safety notice

ASSEMBLY, MONITOR

Brazil / Anvisa · BRA · Aug 3, 2001

Key facts

Title ASSEMBLY, MONITOR
Regulator Brazil / Anvisa
Country BRA
Brand EQUIPMENT: INTEGRIS OR MULTIDIAGNOST SYSTEM 1-MONITOR CEILING SUSPENSIONS: (1) MODEL 9896-000-33421, (2) MODEL 9898-000-33422
Manufacturer PHILIPS MEDICAL SYSTEMS NORTH AMERICA 102120 710 BRIDGEPORT AVE PO BOX 860 SHELTON CT 064840917 DISTRIBUIDOR PHILIPS MEDICAL SYSTEMS NEDERLAND
Models 9896-000-33421, 9898-000-33422, 1-MONITOR
Date Aug 3, 2001
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

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