Directions For Use
Agency Approvals
EC REP
Conforms to: UL 2601-1
Certified to: CAN/CSA C22.2 No. 601.1-M90
IEC 601-1
EN60601-1
EN/IEC 60601-1-2
The CE mark on this product indicates it has been tested to and conforms with the
provisions noted in the 93/42/EEC Medical Device Directive.
Authorized EC Representative:
European Regulatory Manager
Welch Allyn, Ltd.
Navan Business Park
Dublin Road
Navan, County Meath, Republic of Ireland
Tel +353 46 90 67700
Fax +353 46 90 67756
Specifications
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