Inventis TIMPANI Manual Del Usuario página 14

Catalog code
Name and address of manufacturer.
Device with applied parts, Type B (IEC 60601-1)
The device emits radio frequency
Mark indicating conformity with Council Directive 93/42/EEC
concerning medical devices (as amended and expanded by
Directive 2007/47/EC) – Class IIa device, notified body 0123
(TÜV SÜD Product Service GmbH).
Under United States federal law, the device can be sold only to
authorized healthcare professionals.
The product is subject to the requirements of Directive
2012/19/EU on waste electrical and electronic equipment
(WEEE). In the event of this product being sold and/or
scrapped, it must not be disposed of as ordinary household or
industrial waste but collected separately.
Do not reuse. Components bearing this mark can be used once
only and must not be reused thereafter.
6
- characters 6-7: year of manufacture ("20" denotes
2020)
- characters 8-13: pro serial number
UDI code