Devices

Brand Name: External Automated Defibrillator Registration. Technical name: EXTERNAL AUTOMATIC / SEMI-AUTOMATIC DEFIBRILLER. ANVISA registration number: 80102511545. Risk class: III - High Risk. Affected Model: LIFEPAK 1000

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Medical devices help to diagnose, prevent and treat many injuries and diseases. We are not suggesting or implying that any companies or other entities included in the International Medical Devices Database engaged in unlawful conduct or otherwise acted improperly. The same device may have different names in different countries. This database is not intended to provide medical advice and patients should check with their doctors to determine if it contains relevant information and if such information has medical implications for them.

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Brand Name: External Automated Defibrillator Registration. Technical name: EXTERNAL AUTOMATIC / SEMI-AUTOMATIC DEFIBRILLER. ANVISA registration number: 80102511545. Risk class: III - High Risk. Affected Model: LIFEPAK 1000

Manufacturer

VR MEDICAL LTDA; Physio-Control, Inc.