Medical Equipment Classified by Intertek Testing Services NA Inc. with respect to electric
shock, fire, and mechanical hazards only, in accordance with UL 60601-1. Classified under
the Medical Device Directive (93/42/EEC) as a Class IIa device.
Caution, consult accompanying documents.
Conforms to European Medical Device Directive 93/42/EEC.
Manufacture Date (year and month will be inserted below).
China RoHS symbol for products compliance.
B Patient Applied Part according to IEC 60601-1.
GSI Part number and model
Return to authorized representative, special disposal required.
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