International Medical Devices Database

Fuente de la data

País

Clasificación del dispositivo

Empresa matriz

Nombre	Clasificación	Fabricante	Nivel de riesgo	País	Fuente
Spacelabs Healthcare HookUp kits	General and Plastic Surgery Devices	Del Mar Reynolds Medical, Ltd.	1	United States	USFDA
Ultraview SL Command Modules, Model 91496M, upgraded with the Masimo SpO2 Option	Cardiovascular Devices	Spacelabs Healthcare Inc	2	United States	USFDA
Device Recall Spacelabs Healthcare Xhibit Telemetry Receiver, Model 96280, software version 1.1	Cardiovascular Devices	Spacelabs Healthcare Inc	2	United States	USFDA
Device Recall Spacelabs Healthcare Xhibit Telemetry Receiver (XTR)	Cardiovascular Devices	Spacelabs Healthcare Inc	2	United States	USFDA
Device Recall Spacelabs Healthcare Xhibit Central Station	Cardiovascular Devices	Spacelabs Healthcare Inc	2	United States	USFDA
Device Recall 91496 Ultraview SL Command Module	Cardiovascular Devices	Spacelabs Healthcare Inc	2	United States	USFDA
Device Recall Spacelabs Healthcare Xhibit Telemetry Receiver, Model 96280	Cardiovascular Devices	Spacelabs Healthcare Inc	2	United States	USFDA
Device Recall Spacelabs Healthcare Xhibit Central Station	Cardiovascular Devices	Spacelabs Healthcare Inc	2	United States	USFDA
Device Recall Spacelabs qube Compact Monitor, Model 91390	Cardiovascular Devices	Spacelabs Healthcare Inc	2	United States	USFDA
Device Recall Spacelabs Healthcare qube Compact Monitor, Model 91390	Cardiovascular Devices	Spacelabs Healthcare Inc	2	United States	USFDA
Device Recall Spacelabs Healthcare XPREZZON Bedside Monitor	Cardiovascular Devices	Spacelabs Healthcare Inc	2	United States	USFDA
Arkon Anesthesia Delivery System	Anesthesiology Devices	Del Mar Reynolds Medical, Ltd.	2	United States	USFDA
Device Recall Arkon Anesthesia Delivery System, Model 99999.	Anesthesiology Devices	Del Mar Reynolds Medical, Ltd.	2	United States	USFDA
Device Recall Spacelabs Pediatric Flow Sensor Kit	Anesthesiology Devices	Del Mar Reynolds Medical, Ltd.	2	United States	USFDA
Device Recall Model 91393, Xprezzon Bedside Monitor	Cardiovascular Devices	Spacelabs Healthcare, Llc	2	United States	USFDA
Device Recall Spacelabs Healthcare Pathfinder SL Holter Analyzer	Cardiovascular Devices	Spacelabs Healthcare, Llc	2	United States	USFDA
Device Recall Spacelabs Medical Ultraview SL Command Module, Model 91496	Cardiovascular Devices	Spacelabs Healthcare, Llc	2	United States	USFDA
Device Recall Ultraview SL Command Module	Cardiovascular Devices	Spacelabs Healthcare, Llc	2	United States	USFDA
Device Recall Spacelabs Medical Patient Monitor	Cardiovascular Devices	Spacelabs Healthcare, Llc	2	United States	USFDA
Device Recall Vital Sign elance Monitor, Model 93300	Cardiovascular Devices	Spacelabs Healthcare, Llc	2	United States	USFDA
Device Recall Ultraview Spacelabs Medical Multigas Analyzer, Model 91518	Anesthesiology Devices	Spacelabs Healthcare, Llc	2	United States	USFDA
Device Recall Pathfinder Holter Analyzer	Cardiovascular Devices	Spacelabs Healthcare, Llc	2	United States	USFDA
Device Recall Ultraview SL Capnography Module	Cardiovascular Devices	Spacelabs Healthcare, Llc	2	United States	USFDA
Ultraview SL Command Modules with the Masimo SpO2	Cardiovascular Devices	Spacelabs Healthcare Inc	2	United States	USFDA
Device Recall Lifescreen Apnea	Anesthesiology Devices	Del Mar Reynolds Medical, Ltd.	2	United States	USFDA

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Aviso

Los dispositivos médicos ayudan con el diagnóstico, la prevención y el tratamiento de muchas lesiones y enfermedades. A través de la International Medical Devices Database no estamos sugiriendo que compañías u otras entidades mencionadas en la base de datos hayan sido parte de una conducta ilegal o hayan actuado de manera impropia. Un mismo dispositivo médico puede tener distintos nombres en diferentes países. Esta base de datos no busca proporcionar asesoría médica. Los pacientes deben consultar con sus médicos para determinar si la data contiene información relevante y si la misma tiene implicaciones médicas para ellos.