Kaba 90 00 Скачать руководство пользователя страница 2

COF_RegistrationUnits9000-9001-9002_201508_xx

Conformity Standards and directives 

Kaba registration units: 90 01, 90 02 and 90 00

Registration unit 90 01

Registration unit 90 02

Registration unit 90 00

Intended use

Registration units (following called “device”) are used together with electronic control units. 

Registration units are part of a access management system.

The Technical Manual describes the mounting, installation, firmware, functions, 

configuration, putting into operation and maintenance of the device. By consistently 

observing the instructions, you can ensure that the product is used correctly and 

safely. 

This also ensures compliance with the standards and directives in accordance with 

the declaration of conformity.

The Technical Manual is stored on the Kaba Access Control Portal portal.kaba.biz in 

the section Documentation/Enterprise Data Collection/Accesscontrol.

Registered users access this site via their own account, other users via the following 

guest account:

Customer number: (leave blank),  

User name: [email protected], Password: r+pj8c0v

Declaration of conformity

Kaba GmbH, Albertistrasse 3, D-78056 Villingen-Schwenningen hereby declares as the manufac-

turer of the device that the device conforms to the fundamental requirements and other relevant 

stipulations of Directive 1999/5/EC (R&TTE).

The original declaration of conformity is available at  
http://www.kaba.com/access-control/de/Sales-Support/81668/downloads.html?cat=355024

The device complies with the following standards:

EN 60950-1: 2006

+ A11: 2009

Health and safety requirements pursuant to § 3 (1) 1. (Art. 3 (1) a)

EN 301 489-1 V1.8.1

EN 301 489-3 V1.4.1

Protection requirements concerning electromagnetic compatibility

§ 3 (1) 2. (Artikel 3 (1) b)

EN 300 330-1 V1.7.1

EN 300 330-2 V1.5.1

Measures for the efficient use of the radio frequency spectrum

Air interface of the radio systems pursuant to § 3 (2) (Art. 3 (2))

EN60601-1-2: 2007

Registration unit 90 01 only 

Safety and effectiveness of medical electrical equipment

The device complies with the following EC directive: 

R & TTE 1999/5/EC

Radio and Telecommunications Terminal Equipment Directive (R&TTE)

RoHS

To the best of our knowledge, this device does not contain any materials 

(in terms of the concentrations or applications involved) whose circula-

tion within products is prohibited according to the relevant requirements 

under Directive 2011/65/EC (“RoHS”).

Disposal

See Technical Manual

Remove the protective foil.

EN

Quick Guide

Excerpt of the document: TM_RegistrationUnits

Manufacturer

Kaba GmbH

Access Workforce Management

Albertistrasse 3

D-78056 Villingen-Schwenningen

Germany

Tel49 7720 603 0

E-mail: [email protected]

http://www.kaba.com

Отзывы: