Approvals
CM
C
US
74 2 2 7
74 2 2 7
EC REP
N344
CERTIFIED TO: CAN/CSA STD C22.2 NO. 601.1
CONFORMS TO: EN/IEC 60601-1, UL 60601-1,
EN/IEC 60601-1-2, EN/IEC 60601-2-18
The CE mark on this product indicates that it
has been tested to and conforms with the
provisions noted within the 93/42/EEC Medical
Device Directive.
European Regulatory Manager
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
Australia AS/NZS 3200.1
1-12