MKF 2 SW2.4LE-MED GP212

  • Impact-resistant thermoplastic housing, ideal for integration of steute Wireless
  • Wireless signal transmission per steute wireless low energy
  • Power supply via rechargeable Li-Ion battery
  • Socket for recharging of battery
  • LED indication for status
  • Protective bracket
  • Additional push-buttons
  • Different RAL colours
Note
  • Photo shows optional accessories

A true success story in our range of wireless foot controls is the two-pedal MKF 2-MED GP212. Our business unit steute Meditec has been producing this series for several years already, the latest generation with the universal RF SW2.4LE MED technology. This series is built according to wishes of the customer. Options include the integration of additional push buttons and/or a handle for easy positioning. The switch can transmit both analogue and digital signals. Application examples include HF surgery, X-ray and neurosurgery.

Technical data

Applied standardsIEC 60601-1; IEC 60601-1-2; UL 60601; IEC 60529
Pedalshock-proof thermoplastic, UL 94 V-0/V-2
Consoleshock-proof thermoplastic, 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 supplylithium ion rechargeable battery
Mechanical life> 1 million operations
Charging voltage9 VDC – max. 600 mA
 
Performance
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
Frequency range2.4 - 2.4835 GHz
Channel bandwidth2 MHz
Modulation principleGFSK, adaptive frequency hopping of 40 channels
 
Conformity
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

Note

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!