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

Description

250 µL Filtered Universal Pipette Tips – Sterile Boxed Format

Our 250 µL Filtered Universal Pipette Tips are manufactured from high-quality polypropylene (PP), providing reliable performance, high transparency, and precise liquid handling for routine and contamination-sensitive laboratory workflows. Designed for single-channel and multi-channel pipettes, these tips are compatible with most standard micropipettes and provide a versatile solution for a wide range of laboratory applications.

As one of the most common and widely used pipette tip formats, these tips are suitable for routine pipetting operations while providing additional contamination protection for sensitive workflows. The integrated aerosol barrier filter element helps reduce aerosol cross-contamination, liquid backflow, and pipette contamination during liquid handling procedures. The boxed rack format is supplied sterile and suitable for laboratories requiring clean, ready-to-use pipette tips.

Note: These pipette tips are designed for specialized laboratory liquid handling applications. Please verify compatibility with your pipette system 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 250 µL Filtered Universal Pipette Tips are thoroughly tested and certified to meet high industry standards. The integrated aerosol barrier filter helps reduce aerosol contamination and liquid backflow, supporting cleaner and safer liquid handling workflows.

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