The most important electromedical innovation of the last decadesSecond Generation Tecartherapy
Medical Device. Notified Body CE 0120. Directive 93/42/EEC. EN 60601-1:2008 - Medical electrical equipment - Part 1: General requirements for basic safety and essential performance.EN 60601-1-2:2008 - Medical electrical equipment - Part 1-2: General requirements for basic and essential performance - Collateral standard: electromagnetic compatibility - Requirements and tests.
• FrequencySelection:Yes. In need of therapy: 0.8 MHz. 1 MHz. 1.2MHz. • NumberofChannelsAvailable: 1• TypeofTreatments:Intracavitary only. • IntelligentChannel:Yes. The same channel allows treatment with multiple accessories available (device Upgrade
mandatory). • TemperatureMonitoringbySensor: Yes. In MJS Intracavitary device. • SuggestionsofTreatmentbyGuidedProgram:Yes. (Athermal. Thermal. Highly thermal).• BasicorAdvancedScreen:Yes.• ViewingBiofeedbackParameters (absorbedenergy,qualitativeindicationofreal-timepower,coupling,tempe-
rature),toconductclinicalresearch:Yes. • SafetySwitch:Yes. • HygieneSystemsforAccessories: Yes. Probe-cover membrane in latex for intracavitary therapy.
Uro-Gynecological PhysiotherapyTecartherapy - Diathermy
C 500ManualTecartherapy
Electrical Capacitive Transference (Tecartherapy) device forURO-GYNECOLOGICAL Physiotherapy (1 channel)*. MJS Intracavitary device.
* Upgrade your C 500 to C 100.C 500 may be upgraded to C 100: Manual or Automatic Capacitive and Resistive Electrical Transference --TECAR-THERAPY--. With upgrade, treatment becomes extracavitary.
Therapeutic Possibilities
Resistive - RESCapacitive - CAPIsolated
Automatic - AUTOUnattended
Capacitive - CAPIntracavitary electrode MJS
www.capenergy.comThe most important electromedical innovation of the last decades
Second Generation TecartherapyMedical Device. Notified Body CE 0120. Directive 93/42/EEC. EN 60601-1:2008 - Medical electrical equipment - Part 1: General requirements for basic safety and essential performance.EN 60601-1-2:2008 - Medical electrical equipment - Part 1-2: General requirements for basic and essential performance - Collateral standard: electromagnetic compatibility - Requirements and tests.
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Uro-Gynecological PhysiotherapyTecartherapy - Diathermy
C 500
Anal intracavitary in maleVaginal intracavitary in female
Therapeutic combinations
• Upgrade*:Yes.• Power:310 W channel*
• Weight:10,7 Kg• Measurements:34,7 x 42 x 22 cm• IncludesFootstand:No.
Environmental conditionts• Temperature:68ºF-77ºF• RelativeHumidity:<80%
Technical Features
* power established in laboratory on resistive load of 400 ohms.
