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Products

  • Filter integrity tester  Integtest V8.0

    Filter integrity tester Integtest V8.0

    Filter Integrity Tester —— Integtest series
    Dongguan Puno Filter Integrity Tester Integtest series are special instruments of integrity
    testing for sterile filtration membrane and filter system, where the testing method and instrument
    design fully meet the requirements for relevant laws and regulations in GMP, EP, FDA and USP.
    ◎ Regulatory requirements
    1. Chinese GMP and EU EP have made specific provision for the integrity testing of sterile
    filter on the test method, where the commonly used methods include bubble point test, diffusion
    flow test or pressure holding test. GMP regulates that the test is required after the use of sterile
    filtration. EP regulates that the test is required before and after the use, and at the same time EP
    regulates that the critical gas and air filter must be confirmed after use, while other filters must be
    tested on a regular basis.
    2. According to Drug Manufacturing Quality Management Standard (revised in 2010) Article
    310, two appendices of Computerized System and Confirmation and Validation are now issued,
    as the supportive documents for Drug Manufacturing Quality Management Standard (revised in
    2010), effective as of December 1, 2015.
    3. The requirements for electronic records and electronic signatures as specified in 21 CFR
    Part 11.
  • Wireless Glove Integrity Tester (Group Control Edition) | Multi-Device Testing Solution for Pharma & Labs

    Wireless Glove Integrity Tester (Group Control Edition) | Multi-Device Testing Solution for Pharma & Labs

    Boost efficiency with our Wireless Glove Integrity Tester (Group Control Edition). Test multiple gloves simultaneously, ensure ISO compliance, and reduce downtime. Ideal for pharma, labs & cleanrooms. Learn more!

    Wireless Glove Integrity Tester – Group Control Edition
    Advanced Multi-Device Testing for Industrial Glove Quality Assurance

    Our Wireless Glove Integrity Tester – Group Control Edition revolutionizes glove testing for industries requiring stringent quality control. Designed for pharmaceutical labs, cleanrooms, and biotechnology facilities, this system enables simultaneous testing of up to 10 gloves via a centralized wireless interface, ensuring rapid, accurate, and ISO-compliant results.

    Why Choose Our Group Control Tester?
    ✅ Multi-Device Efficiency: Test 6-10 gloves at once, slashing inspection time by 70%.
    ✅ Wireless Connectivity: Eliminate cable clutter with Bluetooth/Wi-Fi-enabled units.
    ✅ Real-Time Monitoring: Track pressure decay, leaks, and test status across all gloves via a 7-inch touchscreen.
    ✅ Compliance Ready: Meets GB/T 25915.7-2010/ISO 14644-7:2004, and GMP standards.
    ✅ Automated Reporting: Generate PDF/Excel reports for audits with customizable templates.

     

     

  • Filter integrity tester  Integtest V8.0

    Filter integrity tester Integtest V8.0

    Filter Integrity Tester —— Integtest series
    Dongguan Puno Filter Integrity Tester Integtest series are special instruments of integrity
    testing for sterile filtration membrane and filter system, where the testing method and instrument
    design fully meet the requirements for relevant laws and regulations in GMP, EP, FDA and USP.
    ◎ Regulatory requirements
    1. Chinese GMP and EU EP have made specific provision for the integrity testing of sterile
    filter on the test method, where the commonly used methods include bubble point test, diffusion
    flow test or pressure holding test. GMP regulates that the test is required after the use of sterile
    filtration. EP regulates that the test is required before and after the use, and at the same time EP
    regulates that the critical gas and air filter must be confirmed after use, while other filters must be
    tested on a regular basis.
    2. According to Drug Manufacturing Quality Management Standard (revised in 2010) Article
    310, two appendices of Computerized System and Confirmation and Validation are now issued,
    as the supportive documents for Drug Manufacturing Quality Management Standard (revised in
    2010), effective as of December 1, 2015.
    3. The requirements for electronic records and electronic signatures as specified in 21 CFR
    Part 11.
  • PES Filter Cartridge for Bio-Pharmaceutical

    PES Filter Cartridge for Bio-Pharmaceutical

    NSS series PES Cartridge are made of Micro series  asymmetric sulfonated

    PES (polyether sulphone) membrane,with universal chemical compatibility,

    PH range 3-11. meeting requirements of latest GMP.

     

  • Sterilizing-Grade PES Membranes Capsule Filters

    Sterilizing-Grade PES Membranes Capsule Filters

    Puno PES capsule filters is family of full size capsule filters

    with various ways of connection at the vent, which enables in-line integrity test.

    The PES membrane bio-burden reduction capsule utilizes single layer hydrophilic

    polyethersulfone membrane. It offers broad chemical compatibility,

    high flow rate and low extractables

    Polyethersulfone is particularly suited for the filtration of products that

    contain substances that adsorb to the media The lower binding characteristics

    of polvethersulfone make it a good choice for filtration of valuable

    protein solutions such as vaccines and biologicals

  • Sterilizing Capsule Filters Asymmetrical PES membrane

    Sterilizing Capsule Filters Asymmetrical PES membrane

    Puno Pes capsule fifilters is family of full size capsule fifilters
    with Staubli connection at the vent, which enables in-line
    integrity test.
    The PES membrane bio-burden reduction capsule utilizes
    single layer hydrophilic polyethersulfone membrane. It offers
    broad chemical compatibility, high flflow rate and low protein absorption rate

    Polyethersulfone is particularly suited for the filtration of products that
    contain substances that adsorb to the media The lower binding characteristics
    of polvethersulfone make it a good choice for filtration of valuableprotein solutions

  • Bio-burden Reduction Capsule filters Hydrophobic PTFE membrane

    Bio-burden Reduction Capsule filters Hydrophobic PTFE membrane

    Capsule filters is family of full size capsule filters with Staubli
    connection at the vent, which enables in-line integrity test.

    The PTFE membrane bio-burden reduction capsule

    utilizes single layer hydrophobic PTFE membrane.

    It offers broad chemical compatibility, high flow rate and low extractables

  • 0.2 micron pes capsule filter

    0.2 micron pes capsule filter

    Capsule filter is that filters cartridge is encapsulated into a self-contained,
    disposable plastic housing, the entire unit is disposable and provide
    significant advantages to the end user.
    disposable capsules do not require emplacement in external steel housings.
    Many of the capsule filters are available in pre-sterilized form, they are readily
    available in various sizes, shapes, and formats consisting of different polymeric
    membranes and can be in a ready to use form on the shelf when needed.
    Although they are disposable, it does not necessarily mean that they are
    more expensive to use as compared to the cartridges.
    The use of disposables entails very little setup time, and virtually no clean up time.

     
    Cleaning validation, which must to be performed with fixed equipment like filter
    housings, is greatly reduced. Puno NSS series capsule filter are designed for
    bio-pharmaceutical, they have various lengths, media and also various types size
    of inlet and outlet are available for practical option

     
  • 0.45um 5″ pp membrane capsule filter for small volume filtration

    0.45um 5″ pp membrane capsule filter for small volume filtration

    Capsule filters are using pleated processing, with compact structure and large filter area, applicable to small flow rate and large volume solutions filtration. Filter are sealed by means of melting, no glues and adhesives so don’t cause any pollution for the filter products. They will experience 100% integrity test, purified water washing, and pressure test before delivery. And there are various materials for selecting and using.

  • Repeated cleaning and recycling titanium sintered tubular filter element

    Repeated cleaning and recycling titanium sintered tubular filter element

    The titanium tubular filter element is made of  high purity titanium powder ,which is ground, sieved , molded and sintered at high temperature and high vacuum. At high temperature, the powder is partially melted and bonded to form a porous structure. the filter element has the advantages of high porosity,excellent mechanicalproperities ,good temperature resistance,excellent chemical compatibility,no shedding, extremely low dissolved substances,repaeted cleaning and recycling , and low operationg cost

  • HFP Particle & Bioburden Reduction Filter Cartridges

    HFP Particle & Bioburden Reduction Filter Cartridges

    HFP filter cartridges were optimized for the wide range of prefiltration. Retention of particles and reduction of bioburden from liquids as well as gases is ensured through fractionated defined depth filtration.This serious filters combine multiple layers of progressively finer pleated polypropylene depth filter material. They are ideally suited for clarification and prefiltration prior to membrane filtration. Key Features ◇ Quick passage rate; large dirt holding capacity, hierarchical interc...
  • Sterilizing-grade filters for the sterile filtration of gases

    Sterilizing-grade filters for the sterile filtration of gases

    Hydrophobic  cartridge filters provide high flow  rate and minimal differential pressure. Cartridges are robust, strong, and resilient and are designed to withstand multiple steam-in-place cycles. Each  cartridge filter is integrity tested during the manufacturing process. A full range of filtration areas is available to suit varying applications and a variety of connection options are offered for easy adaptation to existing housings.   Key Features ◇ Highly safe sterilization, ensuring ...