1000 µL Universal Pipette Tips – Filtered – Extended Length – Sterile Boxed (96/Rack) – Biofargo

Description

Filtered Extended Length Universal Pipette Tips – High-Quality & Wide Compatibility

Our Filtered Extended Length Universal Pipette Tips are manufactured from high-quality polypropylene (PP) material, providing reliable performance, high transparency, and precision liquid handling for routine and contamination-sensitive laboratory workflows. Designed for single-channel and multi-channel pipettes, they 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 offering added protection for sensitive workflows. The extended length design supports easier access into deeper tubes, bottles, and reaction vessels, while the integrated aerosol barrier filter element helps prevent aerosol cross-contamination, liquid backflow, and pipette damage. The boxed rack format is supplied sterile and is suitable for laboratories requiring clean, ready-to-use pipette tips.

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 Extended Length Universal Pipette Tips are thoroughly tested and certified to meet high industry standards. The aerosol barrier filter helps reduce aerosol contamination and liquid backflow, while the extended length design improves access to deeper vessels and helps support cleaner, more controlled pipetting 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