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Device and Product Description ...................................................................1
Contraindications ...........................................................................................1
Safety Information ..........................................................................................1
Instructions for the Patient .................................................................................................. 1
Instructions for the Physician .............................................................................................. 6
Sterilization ......................................................................................................................... 7
EN 60601-1-2 Classification Information ............................................................................ 8
Technical Service ................................................................................................................ 9
End of Programmed Service ............................................................................................... 9
IPG Battery Life .................................................................................................................. 9
Contacting Boston Scientific ............................................................................................. 10
Refer to the Indications for Use for indications and related information.
Refer to the following Directions for Use (DFU) for device specific instructions: Precision
Spectra System Implantable Pulse Generator DFU, Surgical Leads DFU, Percutaneous
Leads DFU, Precision Spectra System Clinician Remote Control DFU, Clinician Trial Manual,
Precision Spectra System Programming Manual, and Programming Wand DFU. Refer to the
Labeling Symbols Addendum for an explanation of labeling symbols.
Refer to the Limited Warranty for warranty information.
Table of Contents
Precision Spectra™ System Information for Prescribers
90668524-11 REV A
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