Certification And State Registration - Nissei WSK-1011 Instruction Manual

9. On the expiry of the specifi ed operation term, refer to specialists (specialized repair organizations) on a periodic basis to check the technical
condition of the device.
10. When utilizing the waste, refer to current rules applicable in your region. No special utilization conditions are specifi ed by the manufacturer
for this device.
11. The cuff is resistant to repeated sanitation. The cuff internal fabric surface (being in contact with a patient' hand) can be treated with a
cotton swab moistened in a 3% solution of hydrogen peroxide. Partial discoloration of the cuff covering tissue is possible if used for a
long time. Do not wash the cuff and do not treat it with a hot iron.

CERTIFICATION AND STATE REGISTRATION

The production of devices is certifi ed pursuant to international standards such as ISO 9001, ISO 13485, ISO 14001:2004.
The device meets international standards IEC60601-1:1988+A1:1991+ A2:1995, IEC60601-1-2:2001+A1:2004/IEC60601-1-2:2007 CISPR
11:2009+A1:2010.
 Complaints and requests should be addressed to:
Little Doctor Europe Sp. z o.o.
57G Zawila Street, 30-390, Krakow, Poland
Service phone: +48 12 2684748, 2684749
Produced by Nihon Seimitsu Sokki Co., Ltd.
Address: 2508-13 Nakago Shibukawa Gunma 377-0293 Japan
Manufacturer: Pt. Nss Indonesia
Address of Manufacturer: Blok A-2 No. 29 St4a Kawasan, Berikat Besland Pertiwi, Kota Bukit Indah Purwakarta 41181, Indonesia
Exporter: Little Doctor International (S) Pte. Ltd.
Address of Exporter: 35 Selegie Road #09-02 Parkline Shopping Centre, Singapore 188307
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