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User Guide
CE Marking:
Documents concerning the conformance of this product to Council Directive
93/42/EEC of 14 June 1993 concerning Medical Devices can be obtained from
Kodak's Health Imaging Division European Representative at:
Kodak GmbH
Product Safety
Phone:
Fax:
DOC:
Canada 1016104159A
¯
This Class A digital apparatus meets all requirements of the Canadian
Interference-Causing Equipment Regulations.
Cet appareil numérique de la Classe A respecte toutes les exigences du Règlement
sur le matérial brouilleur du Canada.
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++49 711 406 2993
++49 711 406 3513
8599110
2004 January Rev. D
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