• Impact-resistant thermoplastic housing, ideal for integration of steute Wireless
  • Wireless signal transmission per steute wireless low energy
  • Power supply via 3 commercially available batteries, type C
  • Battery compartment can be opened by hand
  • Collapsible handle
  • Additional push-buttons
  • LED indication for status
  • Different RAL colours
  • Photo shows optional accessories

The two-pedal wireless foot controls from steute Meditec are true »universalists«, suitable for a wide range of applications. These user interfaces can be adapted to suit the wishes of the customer – for example with additional push buttons or a collapsible handle. The switch can send both analogue and digital signals. Frequent areas of use are mobile X-ray machines and electrosurgery.

Technical data

Applied standardsIEC 60601-1; ANSI/AAMI ES60601-1; IEC 60529
Pedalshock-proof thermoplastic, UL 94 V-0/V-2
Housingshock-proof thermoplastic, UL 94 V-0, RAL 7035
Degree of protectionIP X6 to IEC/EN 60529, up to IP X8 as option
Switching elementsreed contact / micro switch / Hall sensor
Switching system1 – 2 NO contacts
Voltage supply3 commercially available batteries, Typ C
Mechanical life> 1 million operations
Wireless range10 m (typical)
HF data rate1 Mbps
Interface data rate115.2 kBd (UART)
Output power3 dBm - 7 dBm
Input sensitivity-93 dBm
Antennainternal ceramic antenna
Radio technology
Frequency2.4 - 2.4835 GHz
Channel bandwidth2 MHz
Modulation principleGFSK, adaptive frequency hopping of 40 channels
Global IEC 60601-1, -1-2, -2-22, -2-43
Europe EN 300 328; EN 62479; EN 301 489-1; EN 62368-1
USA FCC, Title 47 CFR, Part 15
CanadaIC RSS-247, Issue 1
Japan ARIB STD-16


Since this is a class-2 equipment, the receiver can only be validated together with the complete system of the customer. Thus the assessment of conformity takes place at the customer. At the request of the customer steute can provide a CE mark with the 4-digit number of the customer's notified body.

Application of a CE certified switch conforming to the Medical Device Directive still requires proof of the conformity of the complete system according to the Medical Device Directive (Directive 93/42/EEC) by the person responsible for launching it on the market!