Medtronic DBS Mode D'emploi page 4

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Table of contents
Contraindications 5
Warnings 6
Precautions 8
Physician training 8
Medical procedure coordination 8
Storage and sterilization 8
System implant 9
Device specific considerations 10
Clinician programming 11
Clinician information and general guidance 12
Patient information 14
Adverse events 16
Component disposal 18
This Information for prescribers (IFP) booklet contains disclosure
information applicable to Medtronic DBS therapies. Additional
information, including indication-specific warnings and precautions,
can be found in the IFP addendum. PLEASE REFER TO THE
APPROPRIATE INDICATION-SPECIFIC IFP ADDENDUM FOR
COMPLETE INFORMATION.
Refer to the indications sheet for indications and related information.
Refer to the MRI Guidelines for Medtronic Deep Brain Stimulation
Systems instructions for use manual for the MRI conditions and MRI-
specific contraindication, warnings, and precautions for conducting an
MRI scan.
Refer to the device implant manual for device description, package
contents, device specifications, and instructions for use.
Refer to the System Eligibility, Battery Longevity reference manual for
neurostimulator selection and battery longevity calculations.
Refer to the clinical summary booklet for information on the
clinical study results of the neurostimulation system, individualization
of treatment, adverse events summary, and use in specific
populations.
Information for prescribers 2017-05-01 English 3