hpl 460/660 AP-V
hpl 800/1100/1300 AP-V

SEMI-AUTOMATED HIGH-TECH IMPULSE BAR SEALERS.

hpl 460 / 660 / 800 / 1100 / 1300 AP-V

The impulse bar sealers are ideal for sealing thermoplastic polymer films and aluminium laminate films, as well as for sealing medical packaging in accordance with ISO 11607-1 (EN 868-4/5/9/10). The process is validation-compatible in accordance with the requirements of ISO 11607-2. The machines are designed for high volumes in multi-shift operation. The housing is made from stainless steel and is suitable for use in clean-room environments (special models on request). The sealers are available in bar widths of 450, 630, 770, 960 and 1,160 mm (18, 25, 30, 38 and 46 inches).

hpl 460 to hpl 1300 available in five bar widths.

Available in five bar widths.

 

 

Examples of use:
Packaging of all industrial products, medical products, implants, medicines, pharmaceutical products of all kinds (e.g. header bags), packaging of spare parts in all industries, office requirements, foods, laboratory products, commercial products in wholesale and retail and animal nutrition.

 

hpl 460/660 AP-V
hpl 800/1100/1300 AP-V

Features

  • EASY OPERATION.

    Programming and data input is easy via the control panel, the IntelligentScan system or the optional SealCom Pro communication module. The optionally available ‘bag support device’ allows machines also to be set up at an angle or vertically. 

    ... IntelligentScan >
    ... SealCom PRO >

    hawo SealCom PRO

    Communication module
    SealCom PRO

  •  

    FLEXIBILITY AND PERFORMANCE.

    hawo impulse vacuum sealers have a number of features ensuring that evacuation, gas purge and sealing are user-friendly, safe and easy. The 8 mm (0.3 inch) wide seal seam and the customisable settings options for the process parameters therefore offer maximum flexibility when it comes to choosing packaging materials.
    The impulse bar sealers are equipped with RS 232 interfaces for bidirectional communication as standard.

     
  •  

    DOCUMENTATION SOFTWARE.

    The machines can be equipped with the hawo ProDoc software for legally secure recording of the welding process.

    ... more >

    hawo ProDoc

    hawo ProDoc

Validation

  • Safe packaging.

    The correct reprocessing process of medical devices consists of the steps of washing & disinfection, packaging and sterilisation. The instruments can only be called sterilised when they are packaged before the sterilisation. The single-use (!) packaging, made from laminated poly film and a porous material (Tyvek® or medical grade paper) is permeable for the sterilisation medium (e.g. steam, plasma, Formaldehyde FO or Ethylenoxide ETO), but not for bacteria or microorganisms. Only by following this reprocessing sequence and by using professional heat sealers to seal the instruments as well as professional packaging material can the sterility up to the point of use as well as the aseptic presentation of the instrument be guaranteed.

    Medical devices delivered in a sterile state should be packed to ensure that they remain sterile until the point of use. The validation of packaging processes is crucial to ensure that sterile barrier system integrity is attained and will remain so until opened by the users.

    The international packaging standard ISO 11607-2 as well as the Technical Specification draft ISO/DTS 16775 explain how packaging processes should be validated. The international packaging validation guideline gives guidance how to validate packaging processes. During the validation of the heat sealing process the optimum sealing temperature of the packaging materials used has to be evaluated and established. At this temperature, the process then has to deliver optimum seal seams that are strong enough and peelable.

    Professional heat sealing equipment for closing sealable pouches and reels (preformed sterile barrier systems) are essential for this. hawo therefore offers sealing devices whose processes can be validated according to ISO 11607-2, the Technical Specification draft ISO/DTS 167751 and in harmony with the international packaging validation guideline. The models marked with ‘V’ feature an integrated function for regulating and monitoring process parameters – the ‘V’ is the key! Sealing devices from hawo therefore guarantee efficient and reproducible packing, even for large volumes of instruments.

     

    Definition:

    • IQ Installation Qualification:essential information is checked according to a checklist (e.g. the sealing device is compliant to ISO 11607-2)
    • OQ Operational Qualification: the optimal sealing temperature has to be established
    • PQ Performance Qualification: determination of the seal strength at the optimal sealing temperature determined in the OQ (after sterilisation)

     

     

Downloads

  • Here you can download the
    current PDF brochure.

    Download
    PDF (226 kb)