Atmos MEDAP FINA VAC T 50 Operating Instructions Manual

Atmos MEDAP FINA VAC T 50 Operating Instructions Manual

Tapping unit for drainage

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OPERATING INSTRUCTIONS
TAPPING UNIT FOR DRAINAGE
MEDAP-FINA VAC T 50
GA 5752 3075 GB 13

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Summary of Contents for Atmos MEDAP FINA VAC T 50

  • Page 1 OPERATING INSTRUCTIONS TAPPING UNIT FOR DRAINAGE MEDAP-FINA VAC T 50 GA 5752 3075 GB 13...
  • Page 2 Subject to technical modification! Illustrations and technical specifications may vary slightly from those in these operating instructions as a result of ongoing product development. V13 2020-07 GA 5752 3075 GB 13...
  • Page 3: Table Of Contents

    Symbols used ............................. 6 Disposal ..............................7 1.4.1 Packaging ............................ 7 1.4.2 ATMOS products .......................... 7 Overview ..............................8 1.5.1 Overview of the FINA VAC T 50 ....................8 1.5.2 Overview of the FINA VAC T 50 versions ..................9 Basic requirements .............................
  • Page 4 Table of contents 3.2.2.2 Version A ........................17 3.2.2.3 Version B ......................... 17 3.2.3 Assembly of the septic fluid jar and accessories ............... 18 Operation ..............................20 Function test ............................. 20 Working with the product .......................... 21 Taking the unit out of operation ......................22 Completing the aspiration process ......................
  • Page 5: Introduction

    Your facility has selected the leading-edge medical technology made by ATMOS. We sincerely appreciate the trust you have placed in us. How to use these operating instructions These operating instructions are provided to familiarise you with the features of this ATMOS product. They are subdivided into several chapters. Please note: •...
  • Page 6: Definitions

    Introduction Symbols used 1.2.3 Definitions 1.2.3.1 Design of safety notes Pictogram Descriptor Text The text for the safety note DANGER! describes the type of risk and Indicates a direct and immediate risk to how to avert it. persons which may be fatal or result in most serious injury.
  • Page 7: Disposal

    The packaging is made of materials compatible with the environment. ATMOS will dispose of the packaging materials upon request. 1.4.2 ATMOS products ATMOS will take back used products or those which are no longer in service. Please contact your ATMOS representative for more detailed information. GA 5752 3075 GB 13...
  • Page 8: Overview

    Introduction Overview Overview 1.5.1 Overview of the FINA VAC T 50 1 1 1 1 1 1 0 0 Fig. 1: Overview of the FINA VAC T 50 1 Vacuum gauge 7 Hydrophobic bacterial and viral filter 2 Housing 8 Tube connector of mechanical overflow protection 3 Control valve 9 Mechanical overflow protection 4 Shunt air openings of control valve...
  • Page 9: Overview Of The Fina Vac T 50 Versions

    Introduction Basic requirements 1.5.2 Overview of the FINA VAC T 50 versions Fig. 2: Overview of the FINA VAC T 50 versions 1 Version A 6 Locking lever Tapping unit with integrated gas pin 7 NIST nipple 2 Plug 8 NIST screw connection 3 Terminal unit 9 Connection tube 4 Version B...
  • Page 10: Applicable Standards

    Introduction Basic requirements Accessories Accessories or combinations of accessories may be utilised only as and when indicated in these operating instructions. Other accessories, combinations of accessories and consumable items may be used only if they have a valid certification, are intended expressly for the particular use and will not adversely affect performance, the prescribed ambient conditions or safety requirements.
  • Page 11: Versions

    Introduction Basic requirements Contraindications: The FINA VAC T 50 may not be used for the following purposes: • Outside the medical sector • In MR areas • In the home care sector • Being operated directly by the patient • For vacuum extraction •...
  • Page 12: Interface Description

    Introduction Basic requirements 1.6.5 Interface description All devices and accessories which are combined with the tapping unit must be listed in the accessories list or meet the specifications of the interface description. Configuration of the overall system as well as functional testing are subject to the overall responsibility of the medical staff. Functionality and suitability of the connected accessory for each intended application must be checked by the operator before every use.
  • Page 13: Suction Tube

    Introduction Basic requirements 1.6.5.5 Suction tube The suction tube acts as the connection between the septic fluid jar and the utensil. Technical specifications • Shore hardness of 60 • Inner diameter 6–8 mm • Length 1.3–3.0 m • Vacuum resistant down to −95 kPa (must not collapse) Prerequisites: •...
  • Page 14: Safety Notes

    Risk of injury! ATMOS products may be used only when fully functional . Ensure that this ATMOS product is fully func tional and in good working order prior to use. ATMOS recommends always having another aspirator ready to hand. This enables aspiration even in the event of product failure.
  • Page 15 Safety notes Product safety notes WARNING! Foaming! Foam may be created when extracting secretion. Foam is detrimental to the functioning of the mechanical overflow protection. This raises the risk that secretion may penetrate the product and cause it to break down. Use an ordinary foam inhibitor.
  • Page 16: Initial Operation

    Initial operation Equipment inspection Initial operation Equipment inspection DANGER! Product inspection! Only product parts which are in perfect condition can ensure proper functioning of the product. The product parts will thus have to be carefully inspected before mounting. DANGER! Infection hazard! Contaminated components may be hazardous to the patient's health.
  • Page 17: Connection To The Terminal Unit

    Initial operation Mounting 3.2.2 Connection to the terminal unit 3.2.2.1 General NOTE Please refer to the manufacturer’s instructions for the particular terminal unit for information on connecting the gas probe to the terminal unit. 3.2.2.2 Version A Tapping unit with integrated gas pin ...
  • Page 18: Assembly Of The Septic Fluid Jar And Accessories

    Initial operation Mounting 3.2.3 Assembly of the septic fluid jar and accessories WARNING! Tensile forces! The connected accessories must not exert any mechanical forces which could adversely affect the secure fit of the product. WARNING! Tensile forces! Hold the basic unit with one hand when installing or removing accessories in order to compensate for the tensile forces which are created.
  • Page 19 Initial operation Mounting Connection of the hydrophobic bacterial and viral filter  The connection tubes (1) and (2) are plugged onto the tube connectors of the hydrophobic bacterial and viral filter (3).  Check the flow direction of the bacterial and viral filter.
  • Page 20: Operation

    Operation Function test Operation Function test DANGER! Function check! The product is used in the treatment of patients. Any restriction in the unit's performance can result in serious complications in treatment. Perform a complete function check every time before using the unit. Prior to each use, carry out the following function check: Version A: Tapping unit with integrated gas pin •...
  • Page 21: Working With The Product

    Operation Working with the product Working with the product DANGER! Infection hazard! In the event of oversuction, the hydrophobic bacterial and viral filter must no longer be used. Replace the hydrophobic bacterial and viral filter with a new one. WARNING! Vacuum setting! Make the vacuum settings very carefully! The regulating mechanism is sensitive.
  • Page 22: Taking The Unit Out Of Operation

    Taking the unit out of operation Completing the aspiration process Taking the unit out of operation Completing the aspiration process NOTE Please refer to the manufacturer’s instructions for the particular terminal unit for information on detaching the gas probe from the terminal unit. ...
  • Page 23: Cleaning And Disinfection

    Cleaning and disinfection General Cleaning and disinfection General The product must be wipe or spray disinfected after every use. DANGER! Risk due to incorrect use of detergents and disinfectants! It is strictly advised to observe the manufacturer’s instructions regarding how to use the detergents and disinfectants as well as to observe the valid hospital hygiene rules.
  • Page 24: Cleaning

    Cleaning and disinfection Cleaning Cleaning 6.2.1 General NOTE Use only all-purpose cleaners which are slightly alkaline (soap solution) and contain surfactants and phosphates as the active cleaning agents. In the event of heavily contaminated surfaces, use concentrated all-purpose detergent. CAUTION! Improper cleaning can cause property damage! Residues of physiological saline solutions (e.g.
  • Page 25: Suitable Disinfectants

    Cleaning and disinfection Product-specific safety notes CAUTION! Material damage due to excessive exposure times! Exceeding the specified exposure time of the disinfectant may damage the surfaces. Observe the specified exposure time of the disinfectant manufacturer. 6.3.2 Suitable disinfectants Only surface disinfectants based on the following combinations of active ingredients may be used for disinfection: •...
  • Page 26 Cleaning and disinfection Product-specific safety notes DANGER! Risk to patient! Oversuction of products results in them no longer being functional. There is considerable risk to the patient if the tapping unit is not cleaned properly after being exposed to oversuction, as safety equipment could be clogged. After oversuction, products must be dismantled and cleaned thoroughly by authorised service staff.
  • Page 27: Maintenance

    ATMOS recommends: Work should be carried out by an authorised ATMOS service partner. This ensures that repairs and testing are carried out professionally, original spare parts are used and warranty claims remain unaffected.
  • Page 28: Repairs

    [ page 27]. If defects are detected, the product may not be used any longer. Make a note of the defects and the REF number on the type plate and inform your ATMOS representative. Observe the information in chapter Sending in the device [ page 29].
  • Page 29: Sending In The Device

     Place form QD 434 ‘Delivery complaint / return shipment’ and the respective decontamination certificate in an envelope.  Affix the envelope to the outside of the package.  Send the product to ATMOS or to your dealer. GA 5752 3075 GB 13...
  • Page 30: Technical Specifications

    Technical specifications General Technical specifications General Classification as per Annex IX to Directive 93/42/EEC Class IIa Ambient conditions Temperature: Shipping / storage −15 °C to +50 °C Temperature: Operation +10 °C to +40 °C Relative humidity: Shipping / storage 10% to 95% Relative humidity: Operation 30% to 75% Atmospheric pressure: Shipping / storage...
  • Page 31: Approved Accessories

    Approved accessories Standard scope of delivery Approved accessories Standard scope of delivery 5750 3779 Neutral colour coding label Tab. 7: Standard scope of delivery Accessories 5752 1698 Mechanical overflow protection VAC connection tube with NIST screw connector (see MEDAP tube list) Tab.
  • Page 32 Manufacturer: ATMOS MedizinTechnik GmbH & Co. KG Ludwig-Kegel-Str. 16 79853 Lenzkirch GERMANY Telephone: +49 7653 689-0 www.atmosmed.com...

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