Additional Information - Boston Scientific Vercise Gevia Mode D'emploi

Vercise Gevia™ 16 Contact IPG DFU
Trademarks
All trademarks are the property of their respective holders.
Industry Canada Equipment Certification Number
IC: 9773A-SC1132
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.

Additional Information

For indications, contraindications, warnings, precautions, adverse events summary, physician
instructions, sterilization, component disposal, and warranty information, refer to the Information
for Prescribers DFU. For other device-specific information not included in this manual or labeling
symbols, refer to the appropriate DFU as listed on your DBS Reference Guide.
Product Model Numbers
Model Number
DB-1200
NM-3138-55
SC-4252
SC-4254
Radiopaque Identification Tag
The Stimulator contains a radiopaque identification tag that is visible using standard X-ray
procedures.
Registration of the Vercise Gevia DBS System
In accordance with international practice and regulatory legislation in some countries, a registration
form is packed with each Boston Scientific Stimulator, DBS Lead, and DBS Extension. The purpose
of this form 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.
Vercise Gevia™ 16 Contact IPG DFU
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Description
Vercise Gevia™ 16 Contact Implantable Pulse Generator Kit
55 cm 8 Contact Extension Kit
28 cm Straw Tunneling Tool
35 cm Long Tunneling Tool