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AseptiQuik S Genderless AQS33004

The ASEPTIQUIK S Genderless AQS33004, a 1/4" Sanitary Connector, offers an efficient solution for biopharmaceutical manufacturers needing reliable, sterile connections in small-flow applications. Made from polycarbonate with a USP Class VI, ADCF standard, this connector features a simple "FLIP-CLICK-PULL" design for easy operation, supporting up to 60 psi and temperatures between 39ºF and 104ºF. Its genderless form ensures versatility, requiring no clamps or tube welders for operation.

1 Quantity = 5 Piece Bag 

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AseptiQuik S Genderless AQS33004

The ASEPTIQUIK S Genderless AQS33004 connector epitomizes cutting-edge design in the realm of biopharmaceutical manufacturing equipment. Constructed from durable polycarbonate that adheres to USP Class VI and ADCF standards, this 1/4" Sanitary Connector is specifically engineered to facilitate sterile media transfer in non-sterile environments, crucial for small-flow applications. The molded white material finish, accented with blue tab covers, not only provides visual cleanliness but also indicates its compliance with rigorous health and safety regulations.

This connector's innovative "FLIP-CLICK-PULL" design simplifies the connection process, reducing the likelihood of operator error and accelerating the setup, crucial in high-paced industry settings. By eliminating the need for additional securing hardware such as clamps and tube welders, the AQS33004 ensures a streamlined workflow, enhancing both efficiency and safety. The non-valved, straight bore flow path design allows for direct and unimpeded media transfer, which is ideal for precise operations.

Sterilization is achieved through gamma irradiation, ensuring that the connector remains sterile and ready for use in critical environments. The silicone, platinum-cured seals offer robust performance by maintaining integrity within a temperature range of 39ºF to 104ºF (4ºC to 40ºC), suitable for a variety of bioprocessing tasks. The pressure capacity up to 60 psi further underscores its suitability for demanding applications.

Overall, the ASEPTIQUIK S Genderless AQS33004 is a superior choice for biopharmaceutical manufacturers who prioritize reliability, usability, and compliance. Its genderless interface facilitates universal application, making it a versatile addition to any setup that requires quick, sterile connections without compromising on quality or performance.

Features

  • Genderless Design
  • FLIP-CLICK-PULL
  • Integrated Pull Tab Covers
  • Robust Construction
  • CPC Click
  • 1/4" Sanitary termination with straight bore


Benefits

  • Ease single-use systems specifications with one part number for both halves
  • Intuitive three-step connection process reduces risk of operator error
  • Pull tabs act as protective cover reducing part complexity and ensure simultaneous removal of both membranes
  • Repeatable and reliable performance with no additional hardware required
  • Audible confirmation of assembly
  • Minimizes transitional flow disruptions through upstream processing

Operating Conditions (Fluid Transfer)

Steam Position

Temperature: 39ºF to 104ºF (4ºC to 40ºC)

Pressure: Up to 60 psi, 4.1 bar

Flow Position

Temperature: 39ºF to 104ºF (4ºC to 40ºC)

Pressure: Up to 60 psi, 4.1 bar

Typical Flow Rate: Cv 1.74 for 1/4" to 1/4" and .19 for 1/8" to 1/8"

Main Components: Polycarbonate (white), USP Class VI, ADCF
Pull Tabs/Covers: Polycarbonate (blue, standard version), USP Class VI, ADCF
Polycarbonate (white, HT version), USP Class VI, ADCF
Seals: Silicone (clear), platinum-cured, USP Class VI, ADCF
Membrane: Polyethylene (standard version), USP Class VI, ADCF
Hydrophobic polyethersulfone (HT version), USP Class VI
Termination Sizes
Sizes: 1/8", 1/4" and 3/8" ID hose barb (3.2mm, 6.4mm and 9.5mm),3/4" sanitary and MPC insert
Sterilization
Gamma: Up to 50 kGy irradiation
Autoclave: High Temp (HT) Version:Up to 266ºF (130ºC) for 60 minutes

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At Liquidyne, we prioritize our commitment to quality and consistency. In 2017 we achieved ISO 9001:2015 Quality Management System certification to ensure we can repeatedly deliver consistently high-quality products and solutions. Being ISO 9001:2015 QMS Certified by Orion Registrar, Inc, together with our USP Class VI Testing, ASME Bioprocessing Equipment (BPE), and EHEDG certification guarantee, we have the methodologies to assure quality. We will quickly and accurately rectify any issues if any of our products are ever in non-conformance.

img ‰ files/ISO_9001_Quality_Management_System_Certified.png ¶ url ‰ iso-certificate ¶ cta ‰ View Certificate ¶ txt ‰ At Liquidyne, we prioritize our commitment to quality and consistency. In 2017 we achieved ISO 9001:2015 Quality Management System certification to ensure we can repeatedly deliver consistently high-quality products and solutions. Being ISO 9001:2015 QMS Certified by Orion Registrar, Inc, together with our USP Class VI Testing, ASME Bioprocessing Equipment (BPE), and EHEDG certification guarantee, we have the methodologies to assure quality. We will quickly and accurately rectify any issues if any of our products are ever in non-conformance. ¶
Testimonial from Process Development Manager

"Thanks so much! What a quick turn around. It is a pleasure working with Liquidyne."

Process Development Manager

Testimonial from Vice President, Analytical Development and Manufacturing

"I received the cart yesterday, thanks for the fast delivery! It feels sturdy. I sat on it. It does not bounce. It is also easy to clean and wipe or wash down."

Vice President, Analytical Development and Manufacturing

Testimonial from Chemical Engineer

"Thanks again for reacting so quickly and meeting me halfway with the element. We will be able to get installed and have things keep moving overnight with the night crew. The little things like this are always greatly appreciated when working with Liquidyne."

Chemical Engineer

Testimonial from VP Antibody Manufacturing

“This pump cut our processing time from 3 days to 1 shift. I’m not giving this pump back. You will have to come and get it if you want it... and that won’t likely happen.”

VP Antibody Manufacturing

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