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FAQ
Crédits
Devices
Device Recall EXCITE
Modèle / numéro de série
00000249264MR3, 00000257756MR7, 00000255196MR8, 00000246630MR8, 00000259107MR1, 00000248178MR6, 00000257451MR5, 00000256200MR7, 00000260871MR9, 00000252451MR0, 00000259108MR9, 00000254480MR7, 00000254482MR3, 00000256198MR3, 00000249263MR5, 00000250755MR6, 00000251090MR7, 00000GE0131001, 00000GE0213040, 00000254375MR9, 00000GE0205028, 00000GE0210034, 00000227995MR8, 00000GE0212037, 00000GE0226049, 00000GE0410083, 00000260871MR9, 00000GE0234057, 00000GE0123041, 00000GE0302068
Classification du dispositif
Radiology Devices
Classe de dispositif
2
Dispositif implanté ?
No
Distribution
Worldwide, including USA, China, Finland, Germany, Israel, Italy, Korea, Spain, and Taiwan.
Description du dispositif
GE Healthcare-Americas Signa 3.0T EXCITE Whole Body Magnetic Resonance System
Manufacturer
GE Medical Systems LLC
1 Event
Rappel de Device Recall EXCITE
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Fabricant
GE Medical Systems LLC
Adresse du fabricant
GE Medical Systems LLC, 3200 N Grandview Blvd, Waukesha WI 53188-1693
Source
USFDA
Language
English
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한국어