10 µL Universal Pipette Tips – Filtered – Sterile Boxed (96/Rack) – Biofargo

Description

Filtered Universal Pipette Tips – High-Quality & Wide Compatibility

Our Filtered Universal Pipette Tips are made from high-quality polypropylene (PP) material, ensuring reliable performance and precision liquid handling. Designed for single-channel and multi-channel pipettes, they are compatible with leading brands such as Eppendorf, Gilson, Thermo Fisher, Sartorius, Biohit, Oxford, DLAB, and many other standard pipette brands. These tips provide a versatile solution for a wide range of laboratory applications.

As the most common and widely used pipette tips, they are suitable for routine pipetting operations in research and diagnostic laboratories. The integrated high-quality filter element effectively helps prevent aerosol contamination, liquid backflow, and pipette damage, making them ideal for contamination-sensitive workflows. With a cost-effective design, they provide an economical solution for daily laboratory liquid handling.

Note: Rainin pipettes require specially designed tips and are not compatible with standard universal pipette tips. If you are using a less common pipette brand, please verify compatibility before purchase.

Specifications

Applications

• Pipetting liquids

• Dispensing liquids

• Mixing liquids

• Filling plates and reaction vessels

• Filling gels for electrophoresis

• Phase extraction and removal of supernatants

Competitive Advantage

Our Filtered Universal Pipette Tips are thoroughly tested and certified to meet high industry standards. The integrated filter element effectively reduces aerosol contamination and prevents liquid backflow, helping protect both samples and pipettes during sensitive liquid handling procedures.

Key Certifications & Compliance:

• DNase/RNase Free, Non-Pyrogenic

• Manufactured in a Class 100,000 Cleanroom Environment

• CE Marked and ISO 13485:2016 Certified

• Compliant with the In Vitro Diagnostic Directive (98/79/EC)

• Harmonized Standards:

  • EN ISO 14971:2019 – Risk Management for Medical Devices

  • EN ISO 18113-1:2011 – Information Requirements for IVD Devices

  • ISO 13485:2016 – Medical Device Quality Management System