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15. Symbols

TUV Rhineland of North America is a Nationally Recognized Testing Laboratory (NRTL) in the United States and is accredited by the
Standards Council of Canada to certify electro-medical products with Canadian National Standards.
This product is designed not to become the ignition source in air and flammable anesthetic gas.
The EU directive 93/42/EEC was applied in the design and production of this medical device.
Protected against the effects of continuous immersion in dust and water.
Dispose of this device and its accessories via methods approved for electronic device and in compliance with the Directive 2012/19/
EU.
Type BF applied part
Caution, See Operation Manual
Marking on the outside of Equipment or Equipment parts that include RF transmitters or that apply RF electromagnetic energy for
diagnosis or treatment.
Caution: U.S. Federal law restricts this device to sale by or on the order of a licensed physician
The surface of the product can be used with a Thermo-Disinfector prior to Sterilization.
Single use only. Do not reuse
Authorized representative in the European community
Use by date
EOG sterilization
Batch Code
This product can be sterilized in a steam sterilizer up to Max. 135°C.
Manufacturer
EN15986 Contain of phthalate
Keep dry
This is the correct upright position of the distribution packages for transport and/or storage.
Handle with care
GS1 DataMatrix for Unique Device Identifier.
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