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5. STANDARDS AND DIRECTIVES
The instrument described in this user manual has been designed in compliance with the following
standards:
• ISO 8600-3 First edition 1997-07-01 AMENDMENT 1 Optics and Optical instruments-Medical endo-
scopes and endoscopic accessories Part 3: Determination of field of view and direction of view of
endoscopes with optics.
• ISO 8600-3 First edition 1997-07-01 Optics and Optical instruments-Medical endoscopes and endo-
scopic
Accessories Part 3: Determination of field of view and direction of view of endoscopes with optics.
• ISO 8600-5 First edition 2005-03-15 Optics and phonetics-Medical endoscopes and endotherapy
devices
Part 5: Determination of optical resolution of rigid endoscopes with optics.
• ISO 9001/13485 quality management systems approved by UL(notified body).
• ISO 14971-2007 Risk management to medical devices.
DIRECTIVE USED
• Directives 93/42/EEC, Article II, Section 5, Annex VIII.
• IEC 60601-1-3rd edition (2005)
• IEC 60601-1-2
• EN 55011:2007
CLASSIFICATIONS
• For Europe, per Directive 93/42/EEC, the unit is a Class I instrument, Annex IX.
• For the United States, the FDA classification is Class I.
• Please observe all applicable accident prevention regulations.
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6137000-795
Prima ENT/DNT
Prima ENT/DNT
Issue 1.5
Printed on Feb.26,2019
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