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Crédits
Devices
Device Recall Allura Xper XRay Angiographic
Modèle / numéro de série
Software releases: PBL 10, 20, 30, 40, 50, and 60; CV20; R7.2x; R7.6; R8.1; and R8.2.
Classification du dispositif
Radiology Devices
Classe de dispositif
2
Dispositif implanté ?
No
Distribution
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
Description du dispositif
Philips Medical System Allura Xper X-Ray Angiographic
Manufacturer
Philips Medical Systems, Inc.
1 Event
Rappel de Device Recall Allura Xper XRay Angiographic
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Fabricant
Philips Medical Systems, Inc.
Adresse du fabricant
Philips Medical Systems, Inc., 3000 Minuteman Rd, Andover MA 01810-1032
Société-mère du fabricant (2017)
Philips
Source
USFDA
Language
English
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