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Conformity Standards and directives  

Kaba access manager 92 00

Intended use

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 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: [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 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

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. (Article 3 (1) b)

MIFARE: 

EN 300 330-1 V1.5.1

EN 300 330-2 V1.3.1

LEGIC:

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))

LEGIC:  

EN/IEC 60601-1-2: 2007

Safety and effectiveness of medical electrical equipment

The device complies with the following EC directive: 

1999/5/EG

(R&TTE)

Radio and Telecommunications Terminal Equipment Directive 

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

EN

Quick Guide

COF_AccessManager9200_201406_xx

Excerpt of the document: TM_AccessManager9200

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

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