Hartmann TENSOVAL compact Instrucciones De Uso página 9

13. Legal requirements and 14. Accessories and spare parts
guidelines
To ensure measurement accuracy,
Tensoval compact complies with the only use original HARTMANN acces-
requirements of the EC direc- sories which may be obtained from
tive, 93/42/EEC on Medical devices your pharmacist or specialist med-
and bears the CE-marking. ical supplier.
The device complies with the EN Draw-clamp cuff
1060 standard relating to non-inva- Code No.: 900 179
sive blood pressure monitors Part 1: Upper arm circumference
General requirements EN 1060-1: 22 – 32 cm
1995 and Part 3: Additional require- Pumping bulb
ments for electromechanical blood Code No.: 900 190
pressure measuring systems EN
1060-3: 1997. Clinical testing of
measurement accuracy was
performed according to the testing
protocol recommended by EN 1060-
3 (according to DIN 58130 and
ANSI/AAMI SP10-1992).
Manufacturer:
PAUL HARTMANN AG
89522 Heidenheim
Germany
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