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Stryker RemB - Introduction; Indications For Use; Contraindications

Stryker RemB
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EN 6400-099-700 Rev-AA
Introduction
This Instructions For Use manual is the most comprehensive source
of information for the safe and effective use of your product. This
manual may be used by in-service trainers, physicians, nurses,
surgical technologists, and biomedical equipment technicians.
Keep and consult this reference manual during the life of the
product.
The following conventions are used in this manual:
A WARNING highlights a safety-related issue. ALWAYS comply
with this information to prevent patient and/or healthcare staff
injury.
A CAUTION highlights a product reliability issue. ALWAYS comply
with this information to prevent product damage.
A NOTE supplements and/or clarifies procedural information.
For additional information, especially safety information, or in-
service training, contact your Stryker sales representative or call
Stryker customer service. Outside the US, contact your nearest
Stryker subsidiary.
NOTE: The RemB Electric Universal Driver (handpiece) is also
known as the RemB Universal Driver.
Indications For Use
The Stryker Consolidated Operating Room Equipment (CORE™)
System is intended for use in the cutting, drilling, reaming,
decorticating, shaping, and smoothing of bone, bone cement and
teeth in a variety of surgical procedures, including but not limited
to orthopedic, dental, ENT (ear, nose, throat), neuro, spine, and
endoscopic applications. It is also usable in the placement or
cutting of screws, metal, wires, pins, and other fixation devices.
Contraindications
None known.

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