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INSTRUCTIONS - Olympus

INSTRUCTIONS - Olympus

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Chapter 2 Instrument Nomenclature and Specifications<br />

Medical Device<br />

Directive<br />

This device complies with the requirements<br />

of Directive 93/42/EEC concerning medical<br />

devices. Classification: Class II a<br />

EMC<br />

Applied standard;<br />

IEC 60601-1-2: 2001<br />

This instrument complies with the<br />

standards listed in the left column.<br />

CISPR 11 of emission:<br />

Group 1, Class B<br />

Year of<br />

manufacture<br />

Degree of<br />

protection<br />

against<br />

electric shock<br />

2512345<br />

This instrument complies with the EMC<br />

standard for medical electrical equipment;<br />

edition 2 (IEC 60601-1-2: 2001). However,<br />

when connecting to an instrument that<br />

complies with the EMC standard for<br />

medical electrical equipment; edition 1<br />

(IEC 60601-1-2: 1993), the whole system<br />

complies with edition 1.<br />

The last digit of the year of manufacture is<br />

the second digit of the serial number.<br />

TYPE BF applied part<br />

2.4 Attaching the chain for water-resistant cap<br />

(MAJ-1119)<br />

• Do not lift the endoscope by the chain for water-resistant cap.<br />

Otherwise, operator and/or patient injury can result, or the<br />

endoscope and/or water-resistant cap may be damaged<br />

when fitting part comes off from the S-cord connector mount.<br />

• Do not connect the fitting part to any mount but the S-cord<br />

connector mount. Connecting the fitting part to suction<br />

connector may cause unreliable connection of the suction<br />

tube to the suction connector. It may also cause departing of<br />

the suction tube from the endoscope and the patient debris to<br />

spray.<br />

EVIS LUCERA GIF TYPE 2TQ260M OPERATION MANUAL<br />

19

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