tecartherapy - diathermy c 500 manual tecartherapy · 2018. 4. 6. · c 500 may be upgraded to c...

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The most important electromedical innovation of the last decades Second 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. Frequency Selection: Yes. In need of therapy: 0.8 MHz. 1 MHz. 1.2MHz. Number of Channels Available: 1 Type of Treatments: Intracavitary only. Intelligent Channel: Yes. The same channel allows treatment with multiple accessories available (device Upgrade mandatory).  Temperature Monitoring by Sensor: Yes. In MJS Intracavitary device. Suggestions of Treatment by Guided Program: Yes. (Athermal. Thermal. Highly thermal). Basic or Advanced Screen: Yes. Viewing Biofeedback Parameters (absorbed energy , qualitative indication of real-time power, coupling, tempe- rature), to conduct clinical research: Yes. Safety Switch: Yes. Hygiene Systems for Accessories: Yes. Probe-cover membrane in latex for intracavitary therapy. Uro-Gynecological Physiotherapy Tecartherapy - Diathermy C 500 Manual Tecartherapy Electrical Capacitive Transference (Tecartherapy) device for URO-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 - RES Capacitive - CAP Isolated Automatic - AUTO Unattended Capacitive - CAP Intracavitary electrode MJS

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Page 1: Tecartherapy - Diathermy C 500 Manual Tecartherapy · 2018. 4. 6. · C 500 may be upgraded to C 100: Manual or Automatic Capacitive and Resistive Electrical Transference --TECAR-THERAPY--

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

Page 2: Tecartherapy - Diathermy C 500 Manual Tecartherapy · 2018. 4. 6. · C 500 may be upgraded to C 100: Manual or Automatic Capacitive and Resistive Electrical Transference --TECAR-THERAPY--

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.