Devices

Pulmonary Ventilator Esprit V-100. Anvisa Registration No. 80102510035. Units at Risk: All Esprit V1000 manufactured before December 31, 2004 and Esprit V1000 manufactured prior to Dec 31, 2004 and converted to Esprit V200.

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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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Pulmonary Ventilator Esprit V-100. Anvisa Registration No. 80102510035. Units at Risk: All Esprit V1000 manufactured before December 31, 2004 and Esprit V1000 manufactured prior to Dec 31, 2004 and converted to Esprit V200.

Manufacturer

VR Medical Importadora e Distribuidora de Produtos Médicos Ltda.; Respironics Califórnia, Inc (Ph...