Monitor Maintenance; Warranty Conditions - Hartmann Veroval 9253242 Instructions For Use Manual

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9. Monitor maintenance

Only ever use a soft, damp cloth to clean the monitor. Please
do not use thinner, alcohol, detergents or solvents.
The cuff can be cleaned carefully using a slightly damp cloth
and mild soap solution. Do not completely immerse the cuff
in water.
It is recommended to clean and disinfect the cuff regularly
or after each use, especially when used by several users, to
prevent infection. The cuff should be disinfected, particularly
on the inside, by wiping with a disinfectant. Use a disinfectant
that is compatible with the cuff materials. Keep the monitor in
the storage box to protect it from external influences.

10. Warranty conditions

We offer a 3-year warranty for this premium quality blood
pressure monitor from the day of purchase and in accordance
with the conditions listed below.
Claims must be made during the warranty period. The date of
purchase must be documented by an appropriately completed
and stamped warranty certificate or proof of purchase.
758485-1219_Veroval_Handgelenk-BPM_GB_AR_HK_TR_LB7 2020-03-18.indd 26 758485-1219_Veroval_Handgelenk-BPM_GB_AR_HK_TR_LB7 2020-03-18.indd 26
Within the warranty period, HARTMANN will replace or repair free
of charge any faulty device components caused by material faults or
manufacturing errors. This does not extend the warranty period.
The device is intended for the purpose described in this
instruction manual only.
The warranty does not cover damage resulting from improper
use or unauthorised interference. Accessory parts that are sub-
ject to wear and tear (batteries, cuffs etc.) are excluded from
the warranty. Claims for compensation are limited to the value
of the merchandise; compensation for consequential damage
or injury is expressly excluded.
In warranty cases, please send the monitor with cuff and, if
applicable, the power supply unit, together with the fully com-
pleted and stamped warranty certificate or purchase receipt
directly or via your dealer to the Customer Services depart-
ment for your country.
For patients/users/third parties in the European Union and coun-
tries that are subject to an identical regulatory system (Medical
Device Regulation 2017/745/EU): if a serious adverse reaction
occurs during use of this product or due to using this product,
report this to the manufacturer and/or their authorised represent-
ative and your national authorities.
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