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Product name: MKFS 2PW-MED SH11
Part-number: 1442723
Specification
Metal protective shield in RAL 7035 Lightgrey
Neutral pedal in black
3 m shielded cable
Technical Data
Applied standards
Existing certifications
Protective shield
Pedal
Pedal enclosure
Degree of protection
Contact element and material
Connection type
Mechanical lifetime
Dimension
Weight
Created on: 05.10.2022
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
Sheetmetal in RAL 7035 Lightgrey
shockproof thermoplastic, self-extinguishing / neutral / black
shockproof thermoplastic, self-extinguishing / black
IPX8 (1m / 35 Min.) according to DIN EN 60529
2 micro switches / gold-plated
3 m shielded cable (6xAWG24 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.
155 x 153 x 115 mm
1,0 kg
Revision of data sheet: -
Brückenstraße 91
32584 Löhne, Germany
Phone +49 (0) 5731 745-0
Fax +49 (0) 5731 745-200
D041979
info @ steute.com
www.steute.com
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Summary of Contents for steute MKFS 2PW-MED SH11
- Page 1 Product name: MKFS 2PW-MED SH11 Part-number: 1442723 Specification Metal protective shield in RAL 7035 Lightgrey Neutral pedal in black 3 m shielded cable 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: MKFS 2PW-MED SH11 Part-number: 1442723 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: MKFS 2PW-MED SH11 Part-number: 1442723 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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