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Kaba 9200 Quick Manual page 2

Access manager

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EN
Quick Guide
Conformity Standards and directives
Kaba access manager 92 00
Intended use
The Technical Manual describes the mounting, installation, firmware, functions,
configuration, putting into operation and maintenance of the access manager. 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 Kaba access manager 90 00 conforms to the fundamental require-
ments 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_AccessManager9200_201406_xx
The Kaba access manager 90 00 (following called
"device") is an electronic device for controlling and
monitoring access points within an access manage-
ment system.
It is possible to connect one or two RFID registra-
tion units to an access manager for contactless
reading of RFID tags.
The following registration units can be connected
to the device: Registration unit 90 01, registration
unit 90 02, registration unit 90 00, registration unit
90 000, LA-PP, Kaba exos lock.
Remote and compact readers can be connected to
the RS-485 interface.
There are also two RS-232 interfaces for integrating
Nedap TRANSIT, badge input/output, or system-
dependent functions.
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. (Article 3 (1) b)
MIFARE:
Measures for the efficient use of the radio frequency spectrum
EN 300 330-1 V1.5.1
Air interface of the radio systems pursuant to § 3 (2) (Art. 3 (2))
EN 300 330-2 V1.3.1
LEGIC:
EN 300 330-1 V1.7.1
EN 300 330-2 V1.5.1
LEGIC:
Safety and effectiveness of medical electrical equipment
EN/IEC 60601-1-2: 2007
The device complies with the following EC directive:
1999/5/EG
Radio and Telecommunications Terminal Equipment Directive
(R&TTE)
RoHS
To the best of our knowledge, this device does not contain any mate-
rials (in terms of the concentrations or applications involved) whose
circulation within products is prohibited according to the relevant
requirements under Directive 2011/65/EC („RoHS").
Disposal
See Technical Manual
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_AccessManager9200

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