GE Corometrics 250cx Series Service Manual page 5

Compliance
Components of the
Certified Systems
Component Description
Exceptions
Monitor System EMC:
Immunity Performance
A GE brand Corometrics 250cx Series Monitor bears CE mark CE-0086
indicating its conformity with the provisions of the Council Directive
93/42/EEC concerning medical devices and fulfills the essential
requirements of Annex I of this directive.
The device is manufactured in India; the CE mark is applied under the
authority of Notified Body BSI (0086).
The country of manufacture and appropriate Notified Body can be
found on the equipment labeling.
The product complies with the requirements of standard EN 60601-1-
2 "Electromagnetic Compatibility—Medical Electrical Equipment" and
standard EN 60601-1 "General Requirements for Safety."
The IEC electromagnetic compatibility (EN) standards require
individual equipment (components and accessories) to be configured
as a system for evaluation. For systems that include a number of
different equipment that perform a number of functions, one of each
type of equipment shall be included in the evaluation.
The equipment listed below is representative of all possible
combinations. For individual equipment certification, refer to the
appropriate declarations of conformity.
• 250cx Series Maternal/Fetal Monitor
• Model 146 Fetal Acoustic Stimulator
• Intrauterine Pressure Transducer
• FECG Cable/Legplate
• Ultrasound Transducers (x2)
• Blood Pressure Hose and Cuff
• MSpO Interconnect Cable and Sensor
2
• MECG Cable
• FECG/MECG Adapter Cable
• Remote Event Marker
• RS-232C Interconnect Cables (x3)
• Central Nurses Station Interconnect Cable
• Model 2116B Keyboard and Interconnect Cable
• Model 1563AAO Telemetry Cable
®
• Exergen TAT-5000™
None
Be aware that adding accessories or components, or modifying the
medical device or system may degrade the EMI performance. Consult
with qualified personnel regarding changes to the system
configuration.
CE
0086
CE- i