Iskra Medical d.o.o. of Ljubljana at MEDICA 2019 in Düsseldorf -- MEDICA - World Forum for Medicine
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Iskra Medical d.o.o.

Stegne 23, 1000 Ljubljana
Telephone +386 4 53 25 760
Fax +386 4 53 25 718

Hall map

MEDICA 2019 hall map (Hall 4): stand A19

Fairground map

MEDICA 2019 fairground map: Hall 4

Our range of products

Product categories

  • 04  Physiotherapy / Orthopaedic Technology
  • 04.12  Rehabilitation equipment and devices

Rehabilitation equipment and devices

Our products

Product category: Rehabilitation equipment and devices

Medio CRYO

  • A combination of cold and heat therapies in a single device
  • Adjustable cold therapy temperature: - 4°C to 20°C
  • Adjustable heat therapy temperature: 30°C to 50°C
  • Precise and controlled treatment at a constant temperature
  • Easy and user-friendly operation

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Product category: Rehabilitation equipment and devices

Medio TENS eco

  • Dual-channel battery device with TENS electrical stimulation
  • Portable stimulators for pain relief
  • Recommended for home use
  • Output shapes:
    TENS - Electrostimulation

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Product category: Rehabilitation equipment and devices

Medio MULTI eco

  • Dual-channel device offers multiple types of low- and medium-frequency electrotherapy
  • with 16 different signal shapes
  • 5 standard and 5 adjustable programs for any signal shape
  • Two different therapies can be conducted simultaneously
  • Therapeutic possibilities: Interferential therapy (two-pole and four-pole), Diadynamic currents (MF, DF, CP, LP), Russian muscle stimulation, Muscle stimulation, TENS, EMS, Ionophoresis

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About us

Company details

Iskra MEDICAL is a leading manufacturer of devices for physiotherapy, rehabilitation, and estetic medicine.

Currently, our production assortment includes the electrotherapy, ultrasound, vacuum, laser, pressure, magneto, intense pulse light, and radio frequency equipment, but we constatnly continue to broaden our family of quality medical in cosmetic products.
The starting point in development of a new product is to study the intended purpose of the device, and consider the needs from practitioner’s point of view. The user-friendly operation, efficacy and safety are the main criteria in development. 

The company has a Quality Management System certificate in accordance with ISO 9001 and ISO 13485.

The devices are compliant with EU Medical Device Directive MDD 93/42/EEC and have received an EC certificate through Notified Body 2265 (3EC International).

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