Approvals - Welch Allyn 48700 Operating Instructions Manual

Approvals

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.
Authorized European Representative Address:
European Regulatory Manager
Welch Allyn Ltd.,
Kells Road, Navan,
County Meath, Republic of Ireland.
Tel.: 353-46-79060
Fax: 353-46-27128
NOTE: This product complies with current required standards for
electromagnetic interference and should not present problems to
other equipment or be affected by other devices. As a precaution,
avoid using this device in close proximity to other equipment.
NOTE: This product contains no hazardous materials. Its disposal
will not contaminate or harm the environment, or present any risk
to individuals disposing of the product. As a precaution, it is
recommended you contact your local disposal and/or recycling
authority for information regarding the disposal of the equipment.
20
IEC 60601-1, UL 2601-1, CAN/CSA C22.2 No
601.1, AS3200.1, IEC 60601-1-2
EMC Framework of Australia