Zimmer cryo 6 ремонт

Illustrations Front of the Device Fig. 1 Devices and operating elements 1 Castor 2 Castor guards 3 Control panel 4 Tray 5 Treatment tube connector 6 Treatment tube 7 Container for defrosted water 8 D.

Illustrations Rear of the Device Fig. 2 Devices and operating elements 9 Air filter 10 Mains switch 11 Power inlet 12 Identification plate 9 10 11 12 .

Illustrations Screens and Displays Fig. 3 OK Start/ Stop 10:00 P2 7 P P Operating element display 13 OK key 14 Arrow key for navigation / changing parameters 15 Arrow key for navigation / changing.

Explanation of Symbols In the instructions for use this symbol indicates “Danger”. Caution ! In the instructions for use this symbol indicates „Caution“ with regard to possible damage of the device. Appli.

Contents Illustrations Front of the Device Rear of the Device Screens / Displays Explanation of Symbols Page 1. Indications / Contraindications 1 2. Application Information 2.1 Gen.

Contents 10. Cleaning / Disinfection 25 11. UL — Classification 26 12. Scope of Delivery and Accessories 27 13. Device Combinations 28 14. Safety and Maintenance 14.1 Safety 14.

Indications / Contraindications 1 Seite 1 Indications Cryo 6 cold air device is intended to minimize pain and thermal injury during laser and dermatological treatments and for the temporary topical anesthetic relie.

Application Information 2.1 General 2 Seite 2 Before the device is used on a patient, the user should become acquainted with the operating instructions and individual treatment methods as well as the indications / contra.

Application Information 2.2 Cryotherapy 3 Seite 3 To treat larger areas, the distance from the nozzle to the skin should be increased, resulting in longer treatment times for adequate cooling. At a distance of 5cm.

Warnings 3 Seite 4 Caution! The device may only be used by trained medical personal Caution! After horizontal transport, let the device stand upright for at least 30 minutes prior to switching it on. The cooling agg.

Warnings 3 Seite 5 Do not increase laser output power or energy when using Cryo6 for skin cooling. Skin cooling may reduce effectiveness of some laser treatment on identical power output of the laser. T.

Cryo 6 — in brief 4 Seite 6 What is the Cryo 6? Cryo 6 is used for skin cooling in conjunction with dermatological laser treatments for alleviating pain and thermal damage to skin tissue. What does the Cryo 6 do? .

Intended Use 5 Seite 7 Cryo 6 cold air device is intended to minimize pain and thermal injury during laser and dermatological treatments and for the temporary topical anesthetic relief for injections. .

Device Set Up 6.1 Assembly 6 Seite 8 Caution! After horizontal transport or assembly, the Cryo 6 must stand upright for at least 30 minutes prior to being switched on. The compressor might otherwise be damaged. Con.

Device Set Up 6.1 Assembly 6 Seite 9 To remove the glass plate, reverse these steps. Do not lift the device by the glass plate. Notice: The nozzles for the cold air discharge are .

Device Set Up 6.2 Assembling the Supporting Arm 6 Seite 10 Supporting arm The Cryo 6 device can be optionally equipped with a supporting arm. This arm allows a specific area of the body to be cooled without the therapis.

Device Set Up 6.2 Assembling the Supporting Arm 6 Seite 11 Assembly In order to be able to assemble a support arm, the glass plate must be attached to the device (see 7.1 Assembly). The glass plate has an opening through w.

Device Set Up 6.2 Assembling the Supporting Arm 6 Seite 12 Step 3 – Attach the torsion protection and rod The torsion protection is attached to the glass plate spacers as illustrated. Then, the supporting arm ro.

Device Set Up 6.2 Assembling the Supporting Arm 6 Seite 13 Step 4 – Attach the supporting arm The supporting arm is screwed to the assembled rod (a). To ensure that the supporting arm can move freely up / down, the not.

Settings 7.1 Device Menu 7 Seite 14 After being switched on, the Cryo 6 first performs a self-test. During the self-test and the subsequent pre-cooling of the device, changes can be made in the configuration menu. .

Settings 7.2 Device Type and Device Configuration 7 Seite 15 Device type The Cryo 6 can be operated as «Cryo 6 Physio» and «Cryo 6 Derma». Use the arrow keys (14 and 15) to navigate to the desired pr.

Settings 7.3 Basic Settings and Service 7 Seite 16 Basic settings In this menu option, the factory default settings can be restored. By selecting the «YES» key, all modified parameters will be reset to the fact.

Settings 7.4 Defrosting 7 Seite 17 Defrosting The defrosting process for the heat exchanger is activated under the «Defrost» menu item. Notice: Defrost the device if the discharged air current is weaker t.

Settings 7.5 Own Programs and Favorites 7 Seite 18 Notice: Activating the menus in internal programs, programming 1 and 2-phase programs and the favorite program is only possible if «Programs» is activated as t.

Settings 7.6 Info and Maintenance Programs 7 Seite 19 Info Under this menu point, the technical information about different device components is displayed. Notice: No settings can be made. Maintenance program.

Operating Instructions 8.1 Device Description 8 Seite 20 Pre-cooling Once Cryo6 is turned on, the device starts to pre-cool to the minimum reachable temperature. During this phase, the compressor and the capacitor fan wor.

Operating Instructions 8.2 Performing Cold Treatment 8 Seite 21 Switch on the device Switch the device on using the main switch (10); the display will illuminate. Initialization During initialization, the current sta.

Operating Instructions 8.3 Start Screens 8 Seite 22 Start screens As a factory default, the start screens or start sequence are set differently for the Physio and Derma designs. Start screen Derma / direct start .

Operating Instructions 8.4 Default Parameters / Changes 8 Seite 23 Preset parameters Each unit leaves the manufacturer with a set of standard parameters preset. These may be restored at any time by selecting the “Basic S.

Technical Information 9 Seite 24 Power supply 100 — 120 V / 50 Hz / 60 Hz (9 – 11 A) Power Consumption standby: 2A maximum: 9-11A Mains fuse 16 A circuit breaker in power on/of switch Protection cla.

Cleaning Disinfection 10 Seite 25 — Before starting any maintenance and cleaning measures the device must always be turn off at the main switch and unplugged. — Make sure that during cleaning and disinfection no liquids .

UL-Classification 11 Seite 26 The device bears the following UL Mark: CLASSIFIED BY UNDERWRITERS LABORATORIES INC. WITH RESPECT TO ELECTRIC SHOCK, FIRE, MECHANICAL HAZARDS ONLY IN ACCORDANCE WITH UL 60601-1 AND .

Scope of Delivery / Accessories 12 Seite 27 Scope of delivery 1 Neo light treatment tube 1 Instructions for use 1 Container for defrosted water Accessories Container for defrosted water Neo light tr.

Device Combinations 13 Seite 28 The Cryo 6 can be used in combination with several laser devices. Please follow the operating instructions of the laser manufacturer. Anyone who combines devices and thus operates a med.

Safety and Maintenance 14.1 Safety 14 Seite 29 The Cryo 6 is manufactured in accordance with the safety regulations of DIN EN / IEC 60601-1. Zimmer MedizinSysteme GmbH, as the manufacturer, can only be considered l.

Safety and Maintenance 14.2 Maintenance 14 Seite 30 Cleaning the air filter In order to clean the treatment air and necessary cooling air from dust particles, a filter element (9) is located on the rear of the devi.

Functional Test 15 Seite 31 Functional test After switching on the Cryo 6, it performs a self-test and checks the functionality of the technical components. A functional test of the cooling equipment can be performed b.

Error Messages Troubleshooting Disposal 16 Seite 32 Mains fuse triggers To protect the device from supply problems, the Cryo 6 is equipped with a 2-pole overload fuse integrated into the main switch (10). If the fuse i.

Error Messages Troubleshooting Disposal 16 Seite 33 For other functional faults, please contact the service department. Service department / Distributor Zimmer MedizinSystems 25 Mauchly, Suite 300 Irvine, CA. 9261.

Manufacturer´s EMC declaration 17 Seite 34 With regards to the EMC (electromagnetic compatibility), medical electrical devices such as thr Cryo 6 are subject to special safety measures and must be installed and commiss.

Manufacturer´s EMC declaration 17 Seite 35 Guidelines and manufacturer declaration — electromagnetic interference resistance The Cryo 6 device is intended for operation in the electromagnetic environment indicated below. .

Manufacturer´s EMC declaration 17 Seite 36 with IEC 61000-4-8 Remark: U T is the mains AC voltage prior to applying the test level. Significant performance specifications of the Cryo 6 include: fault-free discharge o.

Manufacturer´s EMC declaration 17 Seite 37 a The field strength of stationary transmitters such as base stations for portable telephones and mobile land radios, wireless keyboard stations, AM and FM radios and televisio.

Источник