LeadCare
®
II User's Guide 1-3
Compliance Statements
CE Mark
IVD - 98/79/EC (27/10/1998) – Annex I and III
EMC
EMC Standard EN 61326-1 (2005) also FCC Part 15 Subpart B Class B
Safety
Complies with:
Low Voltage Directive 2006/95/EC, EN61010-1:2001 (EU) UL61010-1:2004 (USA) CSA
C22.2 No. 61010-1:2004 (Canada) and Requirements for In Vitro Diagnostic (IVD) IEC
61010-2-101:2002.
NOTE:
Protection of this equipment may be impaired if operated in a way not
described in this User’s Guide. Use only the accessories and cables
supplied or specified.
The ETL label on the bottom of the instrument indicates that Intertek Electrical
Testing Labs (ETL) has certified the LeadCare II to the applicable safety
standards.
This device complies with Part 15 of the FCC rules. Operation is subject to the
following two rules:
1. This device may not cause harmful interference.
2. This device must accept any interference received, including interference
that may cause undesired operation.
This device complies with the Waste Electrical and Electronic Equipment
(WEEE) directive of the European Union (EU). For information regarding the
proper decontamination procedure for this product please contact Magellan
Diagnostics. Instruments labeled with the associated symbol (see left) must not
be disposed of as regular waste material.
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