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Product name: KF 1PW-MED GP11
Part-number: 1442726
Specification
Base plate in RAL 7035 Lightgrey with stainless steel bracket
3 m shielded cable
Weight: 1,1 kg
Technical Data
Applied standards
Existing certifications
Base plate
Pedal
Pedal enclosure
Degree of protection
Contact element and material
Connection type
Mechanical lifetime
Created on: 12.11.2021
Page
steute Technologies
1 / 3
GmbH & Co. KG
IEC 60601-1 (Basic Safety)
IEC 60529 (Degrees of protection)
Note: see CSA certificate for corresponding revision level.
CSA
CCC
GD-Al alloy / RAL 7035 Light grey
shockproof thermoplastic, self-extinguishing / black
shockproof thermoplastic, self-extinguishing / black
IPX8 (1m / 35 Min.) according to DIN EN 60529
micro switche / silver-plated
3 m shielded cable (3xAWG20 C UL/CSA RAL 7035)
The expected operating life of the foot switch is limited to 10 years or 1,000,000 switching cycles of the
actuating units, whichever comes first.
Revision of data sheet: -
Brückenstraße 91
32584 Löhne, Germany
Phone +49 (0) 5731 745-0
Fax +49 (0) 5731 745-200
D042057
info @ steute.com
www.steute.com
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Summary of Contents for steute KF 1PW-MED GP11
- Page 1 Product name: KF 1PW-MED GP11 Part-number: 1442726 Specification Base plate in RAL 7035 Lightgrey with stainless steel bracket 3 m shielded cable Weight: 1,1 kg Technical Data IEC 60601-1 (Basic Safety) IEC 60529 (Degrees of protection) Applied standards Note: see CSA certificate for corresponding revision level.
- Page 2 Product name: KF 1PW-MED GP11 Part-number: 1442726 Electrical Ratings max. 25 V AC / 60 V DC Switching voltage (U max. 1 A Switching current (I max. 30 W Switching capacity (P Environmental Conditions Storage/Transport Operating -40 °C up to +70 °C -10 °C up to +60 °C...
- Page 3 Product name: KF 1PW-MED GP11 Part-number: 1442726 General notes The foot switch as a component of a medical device can be evaluated only together in the overall system of the customer. Therefore the conformity evaluation including the classification of the overall system according to the Medial Device Directive 93/42/EEC respectively EU Medical Device Regulation 2017/745 must be carried out at the customer.
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