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ERBE
Diacapsutom
10 / 2000

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  • Page 1 ERBE Diacapsutom 10 / 2000...
  • Page 3 Diacapsutom Instruction manual 10743-000, -001, -002 10 / 2000...
  • Page 4 (including photocopying, microfilm or oth- er means), or processed, reproduced or distributed by means of electronic systems without prior written permission from ERBE Elektromedizin Gm- The information contained in this instruction manual may be revised or ex- tended without prior notice and represents no obligation on the part of ER- BE Elektromedizin GmbH.
  • Page 5: Table Of Contents

    Contents ..........5 Figures ERBE Diacapsutom ........7 Intended use .
  • Page 7: Figures Erbe Diacapsutom

    Figures ERBE Diacapsutom CHAPTER 1: FIGURES ERBE DIACAPSUTOM...
  • Page 8 Fig. 1-1: DIACAPSUTOM front panel. Fig. 1-2: DIACAPSUTOM back. CHAPTER 1: FIGURES ERBE DIACAPSUTOM...
  • Page 9 ERBEBUS. This is a further developed interface system, which has a simple connecting cable. In this way it is possible to operate the DIACAPSUTOM via the footswitch on the ERBE ASPIMAT E. Footswitch socket. Connection for single or dual-pedal foot- switches.
  • Page 10 Figures single-pedal footswitch and accessories Fig. 1-3: Single-pedal footswitch (explosion-proof). Fig. 1-4: Dual-pedal footswitch (explosion-proof). CHAPTER 1: FIGURES ERBE DIACAPSUTOM...
  • Page 11 (Art. nos 20711-008 and 20711-009) or the explosion-proof dual-pedal footswitch (Art. nos. 20743-003 and 20743-004). If activated via the dual- pedal footswitch, the operating mode may be preselected using the black pedal and activated with the gray pedal. CHAPTER 1: FIGURES ERBE DIACAPSUTOM...
  • Page 12 Endodiathermy probe without suction (Art. no. 20738-060) • Bipolar coagulation probe (Art. no. 20738-064) • HF bipolar cable for Art. nos. 20738-054/-060/-064 and 20738-028 CAUTION! Only the accessories listed here may be operated on the ERBE DIACAP- SUTOM. CHAPTER 1: FIGURES ERBE DIACAPSUTOM...
  • Page 13: Intended Use

    • IATHERMY • IATHERMY • APSULOTOMY The unit may be operated as a single unit or together with ERBE phako equipment. 1 and 2 1 and 2: Two programs for bipolar application (bipolar IATHERMY IATHERMY forceps, bipolar pin and endodiathermy. Different intensities may be preprogramed for various intstruments or different applications such as "Wet-Field"...
  • Page 14: Explanation Of The Safety Instructions

    Everyone who prepares, adjusts, works with, dismantles, cleans or disin- instruction manual? fects the unit and instrument set should read the DIACAPSUTOM instruc- tion manual and the instructions for use for the accessories. Please pay par- ticular attention to the safety instructions in every chapter.
  • Page 15 Questions, ERBE If anything is unclear or if you have questions, please contact an ERBE em- Customer Hotline ployee or your local ERBE business office, or use the ERBE Customer Hotline. We would be pleased to assist you and appreciate your suggestions regarding this instruction manual.
  • Page 16 CHAPTER 2: INTENDED USE...
  • Page 17: Maintenance And Care Of The Unit And Accessories

    ERBE detriment of safety. Changes and repairs to the unit must only be performed by the manufacturer or by persons expressly authorized to do this by him in consideration of the special safety requirements for high-frequency sur- gical equipment.
  • Page 18 als. To ensure good radiation of unit heat resulting during operation, air cir- culation must not be impeded. Care of the accessories To protect the accessories from premature wear, the following instructions must be observed: • Do not clean and store forceps with insulated branches together with other hard or pointy instruments, since the insulation may become damaged in this way.
  • Page 19: General Information

    Instructions for the use of high- frequency surgical equipment General information The patient must not come into contact with metal parts that are grounded or have a substantial capacity at ground (e.g. operating table, brackets, etc.). Use of antistatic cloths is recommended for this purpose.
  • Page 20 flammable liquids will collect beneath the patient or in bodily depressions such as the navel or bodily cavities such as the vagina. Liquid that has collected in these locations should be wiped away before using the unit. Warning should be given of the danger of ignition of endogenous gases.
  • Page 21 The unit has not been tested for defibrilation resistance. It is therefore es- sential that no DIACAPSUTOM applied parts be in contact to the patient during defibrilation. CHAPTER 4: INSTRUCTIONS FOR THE USE OF HIGH-FREQUENCY SURGICAL EQUIPMENT...
  • Page 22 CHAPTER 4: INSTRUCTIONS FOR THE USE OF HIGH-FREQUENCY SURGICAL EQUIP-...
  • Page 23: Ambient Conditions

    The DIACAPSUTOM should be operated at a room temperature between +10 °C and +40 °C. Storage, transport ATTENTION! The DIACAPSUTOM should be stored and transported at a room temper- ature between –40 °C and +70 °C. CHAPTER 5: AMBIENT CONDITIONS...
  • Page 24 CHAPTER 5: AMBIENT CONDITIONS...
  • Page 25: Installation Of The Diacapsutom

    Set-up possibilities in the operating room In principle, the DIACAPSUTOM can be set up on tables, ceiling suspend- ed or wall-mounted arm consoles, as well as on special equipment carts. Power connection...
  • Page 26: Explosion Protection

    EN 60601-2-2, § 44.6 aa. Cooling The ERBE Diacapsutom must be set up in such a way that free air circula- tion around the housing is ensured. Therefore setting up in narrow corners, shelves etc. is not permissible.
  • Page 27: Programming The Unit

    Important: The intensity values set remain stored until the next change. In the C program, the intensity need not be set, since the cut- APSULOTOMY ting control provides optimal power for every situation. CHAPTER 6: INSTALLATION OF THE DIACAPSUTOM...
  • Page 28 CHAPTER 6: INSTALLATION OF THE DIACAPSUTOM...
  • Page 29: Testing The Performance

    If properly func- tioning, water vapor results as soon as both tips of the bipolar for- ceps or bipolar electrode contact the sponge. WARNING! The DIACAPSUTOM may only be used when it functions properly in the test. CHAPTER 7: TESTING THE PERFORMANCE...
  • Page 30 CHAPTER 7: TESTING THE PERFORMANCE...
  • Page 31: Working With The Diacapsutom

    Working with the DIACAPSUTOM CHAPTER 8: WORKING WITH THE DIACAPSUTOM...
  • Page 32 Capsulotomy MODE A: Setups Volume 50 % MODE Diath.1 max. 10 s MODE Diath.2 max. 10.0 s MODE MODE Capsulot. max. 60 s Fig. 8-2: Flowchart for changing the set values (see page 34). CHAPTER 8: WORKING WITH THE DIACAPSUTOM...
  • Page 33: Putting Into Operation

    Mode key. Working with the Multifunction footswitch ERBE phako equipment: The unit can be multifunction connected to ERBE phako equipment via the connecting cable (Art. footswitch ERBE no. 20720-019). It is activated using the black key. With the yellow phako equipment key, the operating modes can be selected and acknowledged.
  • Page 34 Pressing again allows you to set the time for the capsulotomy. By pressing the Mode key once again, you return to the application program. To return to the necessary application program, the Mode key must be tapped an appropriate number of times. CHAPTER 8: WORKING WITH THE DIACAPSUTOM...
  • Page 35: Cleaning, Disinfection, Sterilization

    Cleaning, disinfection, sterilization Unit • Clean and disinfect the unit with a spray or wipe-down disinfection. Observe the instructions from the disinfectant manufacturer. • Sterilization of the unit is not possible. WARNING! If cleaning or disinfection of the unit with flammable or explosive agents is unavoidable, they must have completely evaporated from the unit before switching on.
  • Page 36 CAUTION! Aldehydic preparations are better suited for disinfection of electrode han- dles than phenolic agents, since they are less aggressive toward the plastic used. CAUTION! To prevent premature wear, make absolutely certain to observe the instruc- tions from the disinfectant manufacturer regarding soaking time and the concentration of agents used.
  • Page 37: Visual And Acoustic Error Messages

    Visual and acoustic error messages The unit’s microprocessor control systems constantly measure and com- pare all necessary parameters during activation. In this way, the unit func- tions and the generator function are always monitored. If an error is recog- nized, an acoustic warning signal sounds, the HF generator is switched off, and an error message appears on the display.
  • Page 38 CHAPTER 10: VISUAL AND ACOUSTIC ERROR MESSAGES...
  • Page 39: Safety Checks

    Diathermy operating modes. Refer to the technical data (Page 43), the line “HF power output” as a function of the load resistor. • The DIACAPSUTOM high-frequency surgical unit must receive a safety inspection at least once annually. If defects are determined during the safety inspections, which could endanger patients, employees or third parties, the unit must no longer be used until these defects have been rectified by a professional technical service.
  • Page 40 CHAPTER 11: SAFETY CHECKS...
  • Page 41: Guarantee Conditions

    A damage report must be prepared. Unit guarantee The term of the guarantee for the DIACAPSUTOM high-frequency surgi- cal unit is 1 year, calculated from the day of delivery. A guarantee claim may only be made if the correctly filled out guarantee certificate is presented.
  • Page 42 CHAPTER 12: GUARANTEE CONDITIONS...
  • Page 43: Technical Data

    Technical data CHAPTER 13: TECHNICAL DATA...
  • Page 44 Power setting • Cutting (Capsulotomy) automatic • Coagulation (Diathermy) infinite from 1–100 % Activation of HF power Footswitch or ® ERBE BUS Dimensions w×h×d 230×100×330 mm Weight approx. 5.1 kg Operation Temperature +10 °C … +40 °C Relative air humidity 30 % …...
  • Page 45 Storage, transport Temperature –40 °C … +70 °C Relative air humidity 30 % … 95 % CHAPTER 13: TECHNICAL DATA...
  • Page 46 Fig. 13-1: Power with diathermy. CHAPTER 13: TECHNICAL DATA...
  • Page 47 Fig. 13-2: Power with diathermy at 125 Ω. CHAPTER 13: TECHNICAL DATA...
  • Page 48 Fig. 13-3: Power with capsulotomy. CHAPTER 13: TECHNICAL DATA...

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