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Compliant Device
FDA 510(K) Certification
510(K) Number: K091288
WEEE Compliance Statement
Microtek International, Inc. operates under full compliance with the WEEE
Directive. Among the requirements of the Directive are the marking of any
applicable equipment placed in the EU market with the WEEE symbol, a crossed
out wheeled bin as shown at left; demonstration of the implementation of a take-
back program; and meeting recycling targets.
Medi-6000 Plus User's Manual
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