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Vercise™ Deep Brain Stimulation Systems
How to Use this Manual
This manual provides information about the Boston Scientific Deep Brain Stimulation (DBS)
System. Throughout this manual, the name "Boston Scientific DBS System" refers to the following:
Vercise Genus
, Vercise Gevia
, and Vercise
PC Deep Brain Stimulation Systems.
TM
TM
TM
Read all instructions carefully before using the DBS System. For other device‑specific
information not included in this manual, refer to the appropriate Instructions for Use (IFU)
for your Boston Scientific DBS System as listed in your DBS Reference Guide. Advise the
patient that additional information may be available to them on the Boston Scientific website
www.bostonscientific.com/patientlabeling.
Guarantees
Boston Scientific Corporation reserves the right to modify, without prior notice, information relating
to its products in order to improve their reliability or operating capacity.
Drawings are for illustration purposes only.
Trademarks
Vercise™, Vercise Gevia™, Vercise Genus™, SureTek™, and ImageReady™ are trademarks of
Boston Scientific Corporation or its affiliates.
All other trademarks are the property of their respective owners.
The Bluetooth® word mark and logos are registered trademarks owned by the Bluetooth SIG, Inc.
and any use of such marks by Boston Scientific Corporation is under license.
Warranty
For device warranty information, visit www.bostonscientific.com/warranty.
Summary of Safety and Clinical Performance
For customers in the European Union: visit https://ec.europa.eu/tools/eudamed to view a summary
of this device's safety and clinical performance information on the EUDAMED website.
Technical Support
There are no user serviceable parts. If you have a specific question or issue, contact your sales
representative. To contact Boston Scientific for any other reason, use the contact information
provided for your locality via www.bostonscientific.com.
Registration Information
Device registration information must be provided to Boston Scientific following device implantation.
The purpose of this registration is to maintain traceability of all products and to secure warranty
rights. It also allows the institution involved in the evaluation or replacement of a specific implanted
DBS Lead, accessory, or device to gain quick access to pertinent data from the manufacturer. To
complete device registration, follow the instructions provided by your local sales representative.
Patient Implant Card
Following surgery, ensure the patient receives an Implant Card that identifies their particular
implant. Advise the patient to carry the Implant Card with them at all times and to present the
Implant Card to all of their healthcare providers.
Information for Prescribers
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