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Preguntas frecuentes
Créditos
Devices
Device Recall Allura Xper XRay Angiographic
Modelo / Serial
Software releases: PBL 10, 20, 30, 40, 50, and 60; CV20; R7.2x; R7.6; R8.1; and R8.2.
Clasificación del producto
Radiology Devices
Clase de dispositivo
2
¿Implante?
No
Distribución
Worldwide Distribution - USA nationwide including Puerto Rico, Austria, Azerbaijan, Australia, Algeria, Argentina, Albania, Brazil, Belgium, Bangladesh, Bahamas, Bulgaria, Cambodia, Chile, Canada, China, Croatia, Czech Republic, Netherlands, New Zealand, Norway, Oman, Pakistan, Palestine, Panama, Paraguay, Peru, Philippines, Poland, Portugal, Qatar, Romania, Reunion, Singapore, Slovenia, South Africa, Spain, Sudan, Sweden, Saudi Arabia, Switzerland, Syria, Taiwan, Thailand, France, Dominican Republic, Colombia, Turkey, Germany, Greece, Hong Kong, Denmark, Ecuador, Egypt, Estonia, Finland, Vietnam, Russian Federation, Iran, Iraq, Ireland, Israel, Italy, India, Indonesia, Japan, Jordan, Kenya, South Korea, Kuwait, Latvia, Lebanon, Lithuania, Macedonia, Malaysia, Mauritius, Mexico, Moldavia, Mongolia, Morocco, Nepal, Ukraine, United Arab Emirates, and United Kingdom
Descripción del producto
Philips Medical System Allura Xper X-Ray Angiographic
Manufacturer
Philips Medical Systems, Inc.
1 Event
Retiro De Equipo (Recall) de Device Recall Allura Xper XRay Angiographic
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Fabricante
Philips Medical Systems, Inc.
Dirección del fabricante
Philips Medical Systems, Inc., 3000 Minuteman Rd, Andover MA 01810-1032
Empresa matriz del fabricante (2017)
Philips
Source
USFDA
Language
English
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