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Kaba 90 01 Kurzanleitung Seite 2

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Quick Guide
Conformity Standards and directives
Kaba registration units: 90 01, 90 02 and 90 00
Registration unit 90 01
Registration unit 90 02
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: docu2010en@kbs.kaba.com, 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
COF_RegistrationUnits9000-9001-9002_201508_xx
Registration unit 90 00
The device complies with the following standards:
EN 60950-1: 2006
Health and safety requirements pursuant to § 3 (1) 1. (Art. 3 (1) a)
+ A11: 2009
EN 301 489-1 V1.8.1
Protection requirements concerning electromagnetic compatibility
EN 301 489-3 V1.4.1
§ 3 (1) 2. (Artikel 3 (1) b)
EN 300 330-1 V1.7.1
Measures for the efficient use of the radio frequency spectrum
EN 300 330-2 V1.5.1
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.
Manufacturer
Kaba GmbH
Access Workforce Management
Albertistrasse 3
D-78056 Villingen-Schwenningen
Germany
Telephone +49 7720 603 0
E-mail: awm.info@kaba.com
http://www.kaba.com
Excerpt of the document: TM_RegistrationUnits

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Diese Anleitung auch für:

90 0290 00