Closed Male Luer 12C009

  • Closed Male Luer 12C009
  • Closed Male Luer 12C009
  • Closed Male Luer 12C009
  • Closed Male Luer 12C009
  • Closed Male Luer 12C009
  • Closed Male Luer 12C009
  • Closed Male Luer 12C009

Closed Male Luer 12C009

Description Comply with ISO 80369-7 standards, universal design.
Simple mechanism design
Easy to clean swabable surface.
100 PSI pressure compatibility
Pass biocompatibility test
Patented model designs with multiple countries' patents.
Model : 12C009

  • 12C009
  • 12C009 is a closed male luer designed for Gen2 products and other types of NFC (needle-free connector), facilitating easy connection and drug transfer.
  • It features a passive closing function, allowing the connection to open only when connected to female luer lock connectors.
  • Upon disconnection, it incorporates a function to absorb any residual drugs, enhancing safety and minimizing waste.

  • Description Comply with ISO 80369-7 standards, universal design.
  • Simple mechanism design
  • Easy to clean swabable surface.
  • 100 PSI pressure compatibility
  • Pass biocompatibility test
  • Patented model designs with multiple countries' patents.
  • Volume
    • Total length*maximum diameter 36.3mm * 12.75mm
  • Number of parts
    • Assembled with 4 components
  • Surface residue
    • Connect with Gen2 connector P/N:12C007 or other brands
  • Thread matching
    • Conform to ISO 594
  • Pressure Test
    • The maximum operating pressure to bear on 200psi
  • Residual
    • The internal residual of after the operation is completed0.24ml 
  • Flow Rate
    • 80ml/min, higher than the patient's head more than 90CM.


High-Risk Procedures Demanding Rigorous Standards:
  • Chemotherapy infusion and drug preparation are high-risk medical procedures due to the toxicity of chemotherapy drugs.
  • Strict adherence to safety and quality standards, such as USP 797, is essential to protect patients and healthcare professionals.
USP 797: International Standards for Sterile Medication Preparation:
  • Sets comprehensive guidelines for compounding and infusion processes.
  • Focuses on ensuring safety, quality, and hygiene.
  • Covers facility requirements, staff protocols, and risk mitigation measures.
Facility Requirements (USP 797):
  • Clean, orderly, and well-maintained environment.
  • Easy to clean and disinfect.
  • Proper equipment and supplies.
  • Measures to prevent contamination (dust, splashes, etc.).
Staff Protocols (USP 797):
  • Sterile technique usage.
  • Prevention of cross-contamination.
  • Accurate labeling of medications.
  • Understanding of high-risk procedures.
Global Standards and Regulations:
  • Healthcare institutions should comply with local and international standards, including potential additional requirements in their region.
Role of Closed System Transfer Devices (CSTDs):
  • Closed systems that transfer chemotherapy drugs from original packaging to infusion components.
  • Help reduce contamination and risks during compounding and infusion.
  • Aligned with USP 797 principles.
Flexibility in Product Selection:
  • USP 797 provides guidelines but allows flexibility for healthcare institutions to choose products that meet their specific needs and standards.
Chifeng's Solutions:
  • Offers products, including closed male luers and other components, designed to protect healthcare professionals during chemotherapy procedures.
  • Products align with USP 797 guidelines.
  • Contribute to maintaining a sterile and safe environment.
Additional Considerations:
  • Regular staff training and competency assessment.
  • Comprehensive quality management systems and audits.
  • Use of products and equipment that meet USP 797 standards.
  • Robust documentation and reporting systems.