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Manufacturers
Philips Medical Systems Ltda; Philips Medical Systems Nederland B.V
Manufacturer Parent Company (2017)
Philips
Source
ANVSANVISA
1 Event
Safety Alert for Allura Xper Angiography Equipment Technical Name: Angiography Equipment ANVISA Registration Number: 10216710153 Hazard Class: III - High Risk Affected Models: ALLURA XPER FD10 OR table; ALLURA XPER FD20 OR table; ALLURA XPER FD10 (ground); ALLURA XPER FD10 (ceiling); ALLURA XPER FD20 (ground); ALLURA XPER FD20 (ceiling) Series Affected: 45, 53, 139, 170, 180, 123, 263, 173, 174, 195, 179.
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One device in the database
Allura Xper Angiography Equipment Technical Name: Angiography Equipment ANVISA Registration Numbe...
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Philips Medical Systems Ltda; Philips Medical Systems Nederland B.V.
Manufacturer Parent Company (2017)
Philips
Source
ANVSANVISA
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