MOQ: | 1 |
Price: | To be quoted |
Standard Packaging: | safety carton pack or plywood box |
Delivery Period: | 7 working days |
Payment Method: | T/T |
Supply Capacity: | 50 pcs per month |
ISO80369-7-Figure C.1 Female reference luer lock connector for testing male luer connectors for leakage, separation from unscrewing, stress cracking and non-interconnectable characteristics.
Our ISO 80369-7 Figure C.1 compliant female reference luer lock connector is the industry-standard testing device specifically designed for evaluating male luer connectors according to international medical standards. This precision-engineered luer lock testing equipment enables comprehensive assessment of leakage testing, separation resistance from unscrewing, stress cracking evaluation, and non-interconnectable characteristics verification as mandated by ISO 80369-7 standards.
This medical connector testing device serves as the reference female luer against which all male luer lock connectors must be tested to ensure medical device safety and compliance. The ISO 80369-7 Figure C.1 test connector is manufactured to exact specifications for luer lock connection testing and medical fluid pathway evaluation.
Key Features
FAQ
A: The ISO 80369-7 Figure C.1 female reference luer lock connector serves as the standardized testing interface for evaluating male luer connectors regarding leakage resistance, separation force during unscrewing, stress cracking susceptibility, and non-interconnectable characteristics as specified in the ISO 80369-7 standard.
A: This luer lock testing device enables four critical evaluations: Leakage testing of male luer connections, Separation resistance during unscrewing maneuvers, Stress cracking assessment of connector materials, Verification of non-interconnectable characteristics with incompatible connectors.
A: For accurate medical device testing results, we recommend annual calibration verification of your ISO 80369-7 test fixture. The connector should be replaced if any wear, damage, or dimensional deviation is observed that might affect testing accuracy.
MOQ: | 1 |
Price: | To be quoted |
Standard Packaging: | safety carton pack or plywood box |
Delivery Period: | 7 working days |
Payment Method: | T/T |
Supply Capacity: | 50 pcs per month |
ISO80369-7-Figure C.1 Female reference luer lock connector for testing male luer connectors for leakage, separation from unscrewing, stress cracking and non-interconnectable characteristics.
Our ISO 80369-7 Figure C.1 compliant female reference luer lock connector is the industry-standard testing device specifically designed for evaluating male luer connectors according to international medical standards. This precision-engineered luer lock testing equipment enables comprehensive assessment of leakage testing, separation resistance from unscrewing, stress cracking evaluation, and non-interconnectable characteristics verification as mandated by ISO 80369-7 standards.
This medical connector testing device serves as the reference female luer against which all male luer lock connectors must be tested to ensure medical device safety and compliance. The ISO 80369-7 Figure C.1 test connector is manufactured to exact specifications for luer lock connection testing and medical fluid pathway evaluation.
Key Features
FAQ
A: The ISO 80369-7 Figure C.1 female reference luer lock connector serves as the standardized testing interface for evaluating male luer connectors regarding leakage resistance, separation force during unscrewing, stress cracking susceptibility, and non-interconnectable characteristics as specified in the ISO 80369-7 standard.
A: This luer lock testing device enables four critical evaluations: Leakage testing of male luer connections, Separation resistance during unscrewing maneuvers, Stress cracking assessment of connector materials, Verification of non-interconnectable characteristics with incompatible connectors.
A: For accurate medical device testing results, we recommend annual calibration verification of your ISO 80369-7 test fixture. The connector should be replaced if any wear, damage, or dimensional deviation is observed that might affect testing accuracy.