Physiomed PHYSIOTHERM-S User manual

4.5 (2)

S E R V I C E M A N U A L

PHYSIOTHERM-S

Revision: 09 / 2008

Table of Contents

1 GENERAL

3

1.1

Packaging / Transport

4

1.1.1

Transporting the Unit

4

1.1.2

Unpacking the Unit

4

1.1.3

Packing the Unit

4

1.2

Notes on Safety

5

1.3

Service Principle

5

2 TECHNICAL DESCRIPTION

6

2.1

Technical Data

6

2.2

Circuit Description

7

2.3

Power Supply with PCB Input

7

2.4

PCB Power Supply

7

2.4.1 Power Setting – PCB Power Supply

9

2.5

HF Signal Generator

10

2.6

Preliminary Amplifier

10

2.7

Power Amplifier

10

2.8

Output Circuit

11

2.9

Operating Panel

11

3 MOUNTING AND DISMOUNTING ELEMENTS AND PARTS

12

3.1

Elements

12

3.2

Spare Parts

13

3.3

Opening and Closing the Unit

15

3.4

Exchanging PCB Controller, Display and Key Pad

16

3.5

Exchanging the Signal Generator and the Preliminary Amplifier

16

3.6

Exchanging the Power Amplifier

17

3.7

Exchanging the Output Circuit

17

3.8

Exchanging the Tuning Element

18

3.9

Exchanging the Power Switch

18

3.10

Exchanging the Power Supply

18

3.11

Exchanging the Anode/Control Transformer

19

4

SERVICE SETTINGS AND CHECKS

21

 

4.1

The Service Menu

21

 

4.1.1 Activating the Service Menu

21

 

4.2

Manufacturer recommendations on safety inspections according to 93/42 EEC

22

 

4.3

Visual Inspections and Function Checks

22

 

4.4

Setting the Output Power (PCB power supply)

23

 

4.5

Setting the Voltage of the Input Circuit

24

5

ERROR DIAGNOSIS PHYSIOTHERM-S

25

General

1 General

With PHYSIOTHERM-S you have acquired a high-quality and extremely versatile unit for short wave therapy. The most remarkable features of PHYSIOTHERM-S are its convenient operation and modern design as well as its easy maintenance and servicing and high degree of reliability.

The integrated safety functions for improving patient safety more than fulfill legal requirements. The unit is CE-labelled and thus meets the basic requirements laid down in the EC regulations for medical products.

Please note that this Service Manual was established on the basis of the Operating Instructions. Important notes on handling and operating the unit are contained in the Operating Instructions.

If your PHYSIOTHERM-S is in need of service, please contact:

PHYSIOMED ELEKTROMEDIZIN AG

Hutweide 10

D-91220 Schnaittach / Laipersdorf (Germany)

Phone +49 (0) 9126 2587-0

Fax +49 (0) 9126 2587-25

In case of technical problems or if you have technical questions, please contact your local distributor or the address mentioned above.

The unit may only be maintained by PHYSIOMED ELEKTROMEDIZIN AG or an authorized dealer.

If you ever need to return the unit to your dealer or to PHYSIOMED ELEKTROMEDIZIN AG, the original packaging needs to be used. The following information needs to be included:

owner's name and address

serial and device number

description of the error (including error code)

PHYSIOTHERM-S- Service Manual

3

General

1.1 Packaging / Transport

1.1.1Transporting the Unit

In order to ensure save transportation of PHYSIOTHERM-S, the original packaging should be used for transportation. This particular packaging offers the protection required for the transport of the unit in an upright position. Protection is not ensured for flat transportation, which may result in the unit being damaged and impaired in its function.

The authorized dealer or the owner is responsible for proper packaging and needs to ensure that all safety and accident prevention requirements are met.

1.1.2Unpacking the Unit

The unit is generally delivered with the packaging material supplied by the manufacturer. Since the unit's weight is about 60 kg, it must be unpacked by at least two people!

Proceed as follows:

Position the transport packaging so that the UP mark is pointing upward.

Remove the safety straps from the transport packaging.

Lift the upper part of the transport packaging and remove it from the unit.

Remove the top part of the foam material.

Lift (at least two people) the unit from the lower part of the packaging.

1.1.3Packing the Unit

The unit should always be transported in its original packaging. Since the unit's weight is about 60 kg, it must be packed by at least two people!

Proceed as follows:

Bend down both electrode arms.

Affix the lower part of the transport packaging to the pallet.

Place the bottom part of the foam material into the lower part of the transport packaging, the square cut-out facing up.

Put the unit into the square cut-out (at least two people are required!) of the bottom part of the foam material.

Pack all accessories separately. They may be placed in the space left by the unit (between the case and the operating panel) and shipped within the transport packaging.

Place the protective cover (if available) over the unit.

Now place the top part of the foam material over the unit.

Put the upper part of the transport packaging over the unit packed in the foam material and slide it over the lower part of the packaging.

Secure the complete packaging (upper + lower part of packaging + pallet) with safety straps.

4

PHYSIOTHERM-S - Service Manual

General

1.2 Notes on Safety

Some parts within the unit are directly connected to the electric supply system. For some service work it may be required to operate PHYSIOTHERM-S while the unit is open and conduct measurements and settings. For this purpose, the usual safety regulations for preventing electric shock need to be observed.

During operation, voltages of up to several thousand volts are produced in the electric wiring system and the high frequency generator. In particular, the high-voltage supply unit, the tube power amplifier and the transformers may carry currents against electric earth that could result in electric shock.

For use of this Service Manual, knowledge of the Operating Instructions is required.

1.3 Service Principle

PHYSIOTHERM-S is of a modular design. All parts can be mounted and dismounted quickly. Electric and electronic modules are plugged in so that no soldering is required. In case an error occurs on a board or a module it will be replaced for a replacement charge, since repair of a board is usually not practicable on site. Repair is carried out at the manufacturer, if feasible. For this reason, no circuit diagrams of the modules are included in this Service Manual.

PHYSIOTHERM-S- Service Manual

5

Technical Description

2 Technical Description

2.1 Technical Data

Mains connection

115 V / 230 V; 50-60 Hz

 

 

set by voltage selector (anode and control transformer)

 

within the unit

 

 

Power line input

without HF output

 

approx. 200 VA

 

with maximum output

approx. 1400 VA

Line fuse (unit)

16 A (115V)

8 A (230V)

Protection class

I

 

 

Class acc. to EC 93/42

IIa

 

 

Type

BF

 

 

HF nominal power

1000 W pulsed mode (at pulse peak)

 

400 W continuous mode

 

Power setting

10 W increments (CW mode)

 

50 W increments (pulsed mode)

Power indication

Amplitude and effective power

Working frequency

27.12 MHz +/- 0.6 %

 

Pulse duration

200 - 600 μs

 

 

Pulse frequency

10 - 300 Hz

 

 

Treatment duration

1 - 60 min

 

 

Design

IEC 601-1, IEC 601-2-3, IEC 601-1-2

Weight

approx. 60 kg

 

 

Dimensions in mm

420 x 970 x 405 (W x H x D)

 

 

conforms to European Council Directive concerning medical

 

devices 93/42 EEC

 

 

6

PHYSIOTHERM-S - Service Manual

Technical Description

2.2 Circuit Description

The electric components of PHYSIOTHERM-S are located beneath the covering plate (operating panel) and on the boards for power supply; preliminary amplifier and signal generator are located behind the casing cover. The boards and all other electric components are connected via a plug connection and flat strip wires. The following functional blocks may be distinguished according to the block diagram on the following page.

2.3 Power Supply with PCB Input

Power is supplied via the mains supply. The supply voltage is directed to the power switch on the left side of the unit via the PCB input (X1).

Power is supplied via the PCB input to the no-heating appliance plug, the power switch and the anode and control transformers.

The voltage selectors for 115 V or 230 V operation are placed in sockets X10 and X3.

Current limitation control transformer: via NTC resistor R12

Current limitation anode transformer: via resistor R1/R2 and relay K1. After current limitation, the resistors are bridged by the switching contacts of relay K1. The LED V3 indicates that the relay K1 has been activated.

Switching anode voltage: via the relay K2 on the primary side of the anode transformer. The LED V4 indicates that the relay K2 has been activated. The relay is controlled by the power supply via the terminal X9.

The anode transformer is connected to the terminals X7 and X8. The thermal switches of the anode and control transformers are connected to the terminals X7 and X8.

2.4 PCB Power Supply

The high voltage generated by the anode transformer is supplied via the terminals X3 and X5.

In the lower range of performance (up to 280 W), the voltage amounts to 700 V AC, and to 1000 V AC in the upper range of performance (above 280 W).

High voltage is rectified, smoothed and increased by the factor 2.5.

Rectified high voltage in the lower range of performance: approx. 1,750 V DC (700 V x 2.5)

Rectified high voltage in the upper range of performance: approx. 2,500 V DC (1,000 V x 2.5)

The PCB power supply generates the grid voltage required for setting the operating point of the tube.

PHYSIOTHERM-S- Service Manual

7

Physiomed PHYSIOTHERM-S User manual

Technical Description

The PCB power supply also generates the rectified and stabilised supply voltages of 5 V, +/- 15 V, + 24 V and the unstabilised voltage of 50 V. These voltages are required for operating the individual modules.

Supply voltages at terminal strip X4 (HF power output 0 Watt / cont.)

Pin

Measuring point

LED

Voltage

(terminal strip)

 

 

 

 

 

 

 

1

MPP5VDC-A

-

4.8 V-5.2 V

 

 

 

 

2

MPP5VDC-AS

-

4.8 V-5.2 V

 

 

 

 

3

MPP5VDC-B

B3

4.8 V-5.2 V

 

 

 

 

4

MPP15VDC

B4

14.4 V-15.6 V

 

 

 

 

5

MPM15VDC

B5

-14.4 V-(-15.6 V)

 

 

 

 

6

MPP24VDC

B4

23 V-25 V

 

 

 

 

7

Earth

-

0 V

 

 

 

 

8

free

-

-

 

 

 

 

9

MPP50VDC

B4

49 V-55 V

 

 

 

 

10

Earth

-

0 V

 

 

 

 

Grid current measuring point at terminal strip X1 (HF power output 400 Watt / cont.)

Pin

Measuring point

Voltage

(terminal strip)

 

 

1

Earth

0 V

2

MPIG-A

0-100 mV

3

free

-

4

MPIG-B

0-100 mV

5

Earth

0 V

Measured with voltmeter between PIN2 and PIN4 (1 mV corresponds to 1 mA)

Anode current measuring point at terminal strip X2 (HF power output 400 Watt / cont.)

Pin

Measuring point

Voltage

(terminal strip)

 

 

1

Earth

0 V

2

MPIA-A

0-400 mV

3

free

-------

4

MPIA-B

0-400 mV

5

Earth

0V

Measured with voltmeter between PIN2 and PIN4 (1 mV corresponds to 1 mA)

8

PHYSIOTHERM-S - Service Manual

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