Risk of minor injuries These installation and operating instructions – NOTICE apply to: Risk of extensive material/property damage CAS 1 REF: 7117-100-50; 7117-100-50E; Other symbols 7117-100-53; 7117-100-54; 7117-100-54E; These symbols are used in the document and on 7117-100-57; 7117-100-59; 7117-100-60;...
Serial number Intended purpose Medical device CAS 1 The CAS 1 Combi-Separator is designed for Health Industry Bar Code (HIBC) continuous separation of liquids and air and for separation of amalgam from the entire waste water from dental treatment units.
Important information The disposable amalgam containers must only The Installation and Operating Instructions ❯ be used once. must be accessible to all operators of the unit at all times. Improper use Specialist personnel Any use of this appliance / these appliances above and beyond that described in the Installa- Operation tion and Operating Instructions is deemed to be...
Important information 2.10 Transport NOTICE The original packaging provides optimum protec- Negative effects on the EMC due to tion for the unit during transport. non-authorised accessories If required, original packaging for the unit can be Use only Dürr Dental parts or accesso- ❯...
CAS 1 ..... . 7117-100-5x separately: Disposable amalgam container ..7117-033-00 CAS 1 .
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Product description Service kit (5-year interval) ..7117-980-30 Information about replacement parts is available from the portal for authorised specialist dealers at: www.duerrdental.net 9000-606-26/30 2103V005...
Product description Technical data CAS 1 Combi-Separator Electrical data Rated voltage 24 AC 24 DC 36 DC Frequency 50 / 60 Rated power Current consumption in stand-by Signal input from the hose manifold 24 AC 50 / 60 24 - 36 DC...
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Product description Network connection Standard IEEE 802.3u Data rate Mbit/s Connector RJ45 Type of connection Auto MDI-X ³ CAT5 Cable type Ambient conditions during storage and transport Temperature °C -10 to +60 Relative humidity < 95 Ambient conditions during operation Temperature °C +10 to +40...
Product description CA 1 Amalgam Separator Electrical data Rated voltage 24 AC 24 DC 36 DC Frequency 50 / 60 Rated power Current consumption in stand-by Signal input from the hose manifold 24 AC 50 / 60 24 - 36 DC Media ³...
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Product description Ambient conditions during operation Temperature °C +10 to +40 Relative humidity < 70 Classification Medical Device Class 9000-606-26/30 2103V005...
Product description CA 2 basic unit Electrical data Rated voltage 24 AC 24 DC 36 DC Frequency 50 / 60 Rated power Current consumption in stand-by Signal input from the hose manifold 24 AC 50 / 60 24 - 36 DC Media ³...
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Product description Ambient conditions during storage and transport Relative humidity < 95 Ambient conditions during operation Temperature °C +10 to +40 Relative humidity < 70 Classification Medical Device Class 9000-606-26/30 2103V005...
Product description Information about the EMC Electromagnetic compatibility (EMC) Interference emission measurements High-frequency emissions in accordance with CISPR 11 Group 1 Class B Interference voltage at the power supply connection Compliant CISPR 11:2009+A1:2010 Electromagnetic interference radiation Compliant CISPR 11:2009+A1:2010 Emission of harmonics Compliant IEC 61000-3-2:2005+A1:2008+A2:2009 Voltage changes, voltage fluctuations and flicker emis-...
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Product description Electromagnetic compatibility (EMC) Interference immunity measurements on the supply input Immunity to fast electrical transients/bursts – AC mains voltage IEC 61000-4-4:2012 Compliant ± 2 kV 100 kHz repetition rate Immunity to surges, line-to-line IEC 61000-4-5:2005 Compliant ± 0.5 kV, ± 1 kV Immunity to surges, line-earth IEC 61000-4-5:2005 ±...
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Product description Electromagnetic compatibility (EMC) Interference immunity measurements on the cover Immunity to electrostatic discharge IEC 61000-4-2:2008 Compliant ± 8 kV contact ± 2 kV, ± 4 kV, ± 8 kV, ± 15 kV air Immunity to high-frequency electromagnetic fields IEC 61000-4-3:2006+A1:2007+A2:2010 3 V/m Compliant...
Product description Type plate The type plates are located on the cover of the motor. Type plate Evaluation of conformity This device has been subjected to conformity acceptance testing in accordance with the cur- rent relevant European Union guidelines. This equipment conforms to all relevant requirements.
Separation The waste water flows through the connection (1) from the spittoon directly into the centrifuge (8) At the inlet connection (3) of the CAS 1, the aspi- and amalgam separation. rated fluid/air mix is accelerated and set into a During the suction phase the aspirated secre- spiral motion in the separation unit (6).
The station selection valve also acts as a safety Operating problems valve. If the CAS 1 is over-full or not functioning If the unit is not ready for operation due to a fault, properly, the system will perform a safety shut- this will be indicated on the display panel via illu- down.
Install an all-pole disconnect switch with a con- ❯ tact opening width of at least 3 mm in the elec- CAS 1 Combi-Separator trical connection to the mains power supply. – Directly in the treatment unit. Observe the current consumption of the devi- –...
Assembly Combination variants Installation type Line layout (minimum requirements) Single-station combination Flexible – PVC data cable with suction unit shielded cable sheath- ing, as used for tele- communications and IT processing systems (e.g. type LiYCY) – Lightweight PVC control cable with shielded cable sheathing Wire cross-section Unit feed:...
In various types, the station selection valve is that such connections can be safely made or if directly mounted on the CAS 1. The station you are in any doubt, always get a suitably selection valve (for separate installation) should qualified person (e.g.
Suction unit Unit in a housing, e.g. next to the treatment unit. Spittoon connections See "Installation information CAS 1 in a housing" In some dental units it is possible that noises can be heard at the spittoon, which are amplified by Installation of the CA 1 next the funnel shape of the spittoon itself.
Signal input from the hose manifold A suitable surge tank is available as a special Rinsing unit or place selection valve / accessory. safety valve (CAS 1 only) (max. 8 W) 24 V DC Power supply CAN bus Display panel, external (X6a = connection...
Rinsing unit or place selection valve / connected if there is no isolation present safety valve (CAS 1 only) (max. 8 W) between the suction unit signal and sta- 24 V DC tion selection valve in the treatment unit.
Assembly Network connection All connected IT units must correspond to the currently-valid edition of IEC 60950. Purpose of the network connection The network connection is used to exchange information or control signals between the unit and a software installed on a computer, in order to, e.
Main PCB (main board) H5 H6 Spannungsversorgung, nach EN 60601‑1 Signaleingang von der Schlauchablage (bei CA 1 + 2 optional) Spüleinheit oder Platzwahlventil / Sicherheitsventil (nur CAS 1) CAN bus Display panel, external (X6a = connection for predecessor model) Sensor technology...
Assembly Commissioning Sensor PCB In many countries technical medical prod- ucts and electrical devices are subject to regular checks at set intervals. The owner must be instructed accordingly. Turn on the unit power switch or the main sur- ❯ gery switch. Carry out an electrical safety check in accord- ❯...
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Assembly Network configuration Various options are available for network configu- ration: ü Automatic configuration via DHCP (recommen- ded). ü Automatic configuration via Auto-IP for direct connection of unit and computer. ü Manual configuration. Configure the network settings of the unit using ❯...
Assembly Every time the service key is pressed, the sedi- 11 Description of the service ment level is checked. If a test collector vessel is used for this, the different levels can be scanned program and made visible on the display panel. While changing the collectors (collector vessel - Wear protective equipment to avoid any test collector vessel ) in the service program the...
Usage 12.3 Amalgam collector vessel is Usage 100% full Yellow LED is on 12 Display/handling Red display flashes Audible signal melody sounds – At a fill level of 100% the signal melody can no longer be switched off by pressing the reset button.
Usage 12.5 Motor fault 13 Disinfection and cleaning Red display and NOTICE green LED flash alternately Device malfunctions or damage due Audible signal to use of incorrect media Guarantee claims may become invalid – Press the reset button briefly to switch off the as a result.
Usage The following are required for disinfection/clean- 14 Replace the amalgam col- ing: lector vessel ü Non-foaming disinfectant/cleaning agent that is compatible with the materials. NOTICE ü Unit care system, e.g. OroCup Risk of contamination if the amalgam To pre-clean, suck up 2 litres of water with the ❯...
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Usage Arrange to have filled amalgam collector ves- ❯ sels collected from the surgery by a local waste management company. New amalgam collector vessels should be ❯ ordered from your specialist dental equipment retailer. Document the replacement and legally compli- ❯...
Usage 15 Maintenance All maintenance work must be performed by a qualified expert or by one of our Service Techni- cians. WARNING Infection due to contaminated unit Clean and disinfect the suction before working on the unit. ❯ Wear protective equipment when working (e. g. impermeable gloves, protective goggles and ❯...
Usage Regulations, Annex 50, Dental Treatment) by an 15.2 Tests inspector in accordance with national regulations. For inspection, the following are required: WARNING ü Test vessel Infection due to contaminated unit ü Measuring beaker Clean and disinfect the suction before ❯...
Troubleshooting Troubleshooting 16 Tips for operators and service technicians Any repairs exceeding routine maintenance may only be carried out by qualified personnel or our service. WARNING Infection due to contaminated unit Clean and disinfect the suction before working on the unit. ❯...
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Troubleshooting Error Possible cause Remedy Device not "ready for opera- The main power switch of the Main power switch ON. ❯ treatment unit or surgery is not tion" No display on the display switched on panel. If an external display panel is fit- Check cable connections.
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Troubleshooting Error Possible cause Remedy Water accumulating in the Coarse sieve in the fluid inlet Clean the coarse sieve. ❯ blocked spittoon Outlet ineffective or not vented Check or retrofit the ventila- ❯ tion. * Suction power too weak or Coarse sieve is blocked on the Clean the coarse sieve.
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Troubleshooting Only by customer services service technicians. 9000-606-26/30 2103V005...
Troubleshooting 17 Transporting the unit 16.1 Replacing the fuse WARNING Prior to working on the unit or in case of danger, disconnect it from the mains. Infection due to contaminated unit Disinfect the unit before transport. ❯ Transformer Close all media connections. ❯...
Appendix Appendix 18 Handover record This document confirms that a qualified handover of the medical device has taken place and that appropriate instructions have been provided for it. This must be carried out by a qualified adviser for the medical device, who will instruct you in the proper handling and operation of the medical device. Product name Order number (REF) Serial number (SN)
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