Batteries and electronic instruments must be disposed of in accordance with the locally
applicable regulations, not with domestics waste.
12.
Reference to Standards
Device standard: Device corresponds to the requirements of the European standard for
non-invasive blood- pressure monitor
EN1060-1
EN1060-3
EN1060-4 – clinical investigation
IEC/EN 60601-1-11
ANSI / AAMI SP10, NIBP,
IEC80601-2-30:2009 + corrigendum 2010
Electrical compatibility: Device fulfils the stipulations of the
IEC/EN 60601-1,
IEC/EN 60601-1-2
The stipulations of the EU-Guidelines 93/42/EEC for Medical Products Class IIa have been fulfilled.
13.
Remark:
Some electrical and electrical
equipments forbid to abandon
and disposal at will
TUV NO.
Manufacturer’s name and
address
Reading Instruction Book before
use
