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The proposed document is addressed to manufacturers of magnetic resonance conditional implantable devices as well as manufacturers of magnetic resonance equipment and pertains to situations in which a patient with an magnetic resonance conditional implant undergoes an magnetic resonance examination.
Reģistrācijas numurs (WIID)
94251
Darbības sfēra
The proposed document is addressed to manufacturers of magnetic resonance conditional implantable devices as well as manufacturers of magnetic resonance equipment and pertains to situations in which a patient with an magnetic resonance conditional implant undergoes an magnetic resonance examination.
