Accu-Chek ACTIVE - Measuring Range and Error Sources

48
Chapter 6: Technical Information ACCU-CHEK Customer Care Service Center 1-800-858-8072
Product S afety Inf or m ation
Explan ation of S y m bols
CA U TI O N
Please refer to safety-related
notes in t he m anual
acco m panying this
instru m ent.
O ne 2032 or equivalent
l ith iu m battery.
The ACC U -C H EK Active m eter
has been listed by
U nderwriter’s L aboratories,
Inc., in accordance with U L
3101- 1 and CA N /C S A C22.2
N o. 1010-1.
This product fulfills the
require m ents of
D irective 98/79/ EC on
in vitro diagnostic
m edical devices.
This product fulfills the
require m ents of
D irective 98/79/ EC on
in vitro diagnostic
m edical devices.
If you need to throw your m eter away:
The European U nion has a require m ent a i m ed at i m proving waste m anage m ent practices for certain electronic equip m ent.
1
This is not a require m ent for
the U S A, however please consider these points if you ever need to dispose of your blood glucose m eter. Any product co m ing in contact with blood is
considered conta m inated ( potentially infectious ) .
2
D uring nor m al testi ng use, any blood glucose m eter m ay co m e in contact with blood. U sers in
professional environ m ents ( e.g., healthcare facilities ) should follow their existing policies and procedures that govern disin fection and/or disposal of
potentially infectious waste. Consu m ers should use appropriate caution if they find a need to dispose their used m eter. W e suggest that you also re m ove
the battery before disposing.
1
D irective 2002/96/EC ( D irective on waste ele ctric a l and electronic equip m ent ( W EEE ) .
2
29 CF R 1910.1030 – Bloodborne pathogens.