About Us

The company 2EL, spol. s r.o. was founded on May 2, 1991. At that time, its activities included assembling computers and installing computer networks, manufacturing cosmetic devices, and already developing, designing, and manufacturing pulsed magnetic therapy devices. In 1994, the computer and medical technology branches became independent, and 2EL, based in Nový Bydžov, began focusing exclusively on pulsed magnetic therapy devices.

Collaboration with specialists MUDr. Jiří Chvojka, CSc., and MUDr. Jiří Jeřábek, CSc., who were pioneers of modern magnetic therapy in our country, led to the company's first successes. As early as 1993, 2EL was included in the European Community's COST 244 project, with the research topic "Design and Clinical Testing of Magnetic Therapy Devices." Through this project, the company gained significant insights into the effects of pulsed magnetic fields on the human body.

Based on these new findings, a revolutionary change was made in the design of magnetic therapy (MGT) devices, notably reducing their energy consumption, optimizing the patient's energy load during treatment, and, paradoxically, simultaneously increasing their therapeutic effectiveness.

At this time, the company became the first in the world to initiate the production of handheld magnetic therapy devices designed for treatment, rehabilitation, and stimulation using pulsed magnetic fields in the home environment. The device "came" to the patient, rather than the patient having to go to the device, as was customary until then. The company has been developing and manufacturing pulsed magnetic therapy devices for 22 years. During this time, it has produced over 130,000 magnetic therapy devices, which reliably serve satisfied customers worldwide.

The production of medical devices in EU member states is subject to Directive 93/42/EEC (the "Medical Directive"), which is harmonized with Czech Government Regulation No. 336/2004 Coll. This law mandates that manufacturers of active medical devices, including magnetic therapy devices, must ensure that each device produced conforms to the certified type. At 2EL, this is ensured through the so-called EC verification of each production series (CE certification). This verification is carried out by the Electrotechnical Testing Institute in Prague, a notified body No. 1014. Products verified in this way are then marked with the CE 1014 European conformity label.