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Differential pressure sensor: ±2kpa, error≤0.5%F.S.
Differential pressure resolution: 0.1pa
Test pressure sensor: Error≤±1%F.S.
Test pressure range: -0.1～0.2MPa/-0.1～0.7MPa/-0.1～1.0MPa
Minimum detectable aperture: 2μm
Display method: 10-inch touch color touch screen
Voltage: AC100V-240V, 50/60Hz, power ≤200W
Weight: Host: about 30kg
Audit trail: ≥5 years of storage Multiple event logs, which can be queried according to time
Authority management: Login with username and password, level 4 authority, meet FDA 21CFR PART 11 requirements
Print function: External micro printer
History record: ≥5 years storage
Data backup: Support U disk to export data
Signal output: (4-20) mA, RS485, 12V alarm output
Interface: Ethernet USB RS485
Product Description:
Packaging leak tester is suitable for sealing integrity testing of pharmaceutical packaging to prevent moisture, oxygen, and microorganisms from contaminating products. Medicines: bottled, bagged, boxed, ampoules, vials, cartridges, prefilled needles (PFS), (BFS), (FFS), etc.
Spray cans: plunger spray cans; bag-lined spray cans; "energy jacket" spray cans; flexible tube spray cans.
Test Standards: USP <1207>, ASTM F2338 standards and FDA standards
Product Features:
◎Comply with USP <1207>, ASTM F2338 standards and FDA standards.
◎Semi-automatic detection, suitable for small batch and multi-variety testing.
◎Non-destructive non-destructive testing, high accuracy, repeatability, sensitivity.
◎The instrument is used for vacuum pressure difference detection.
◎The leak rate can be automatically converted into defect aperture μm.
◎Database storage of test results for easy quality management.
◎Database storage of test results for easy quality management.
◎Touch-type man-machine interface, simple and quick operation: after setting/selecting the test program, only need to manually put in/take out the test sample.
Advantage function:
◎Automatically test the flow rate and change the aperture size during the whole process.
◎Automatic leak rate calibration function.
◎Equipped with standard leaks (standard positive bottles, with third-party certification).
◎Four-level user authority management meets FDA 21CFR PART 11 requirements.
◎With audit trail function.
◎Split design, the test chamber is located above the host, and various test chambers can be provided according to different product types.
◎We also provide users with supporting services related to tightness testing, including positive bottle production, standard leak rate/annual leak verification, new sample mold customization, sample methodological parameter development and verification, etc.
◎The test cavity is customized according to customer needs to ensure that the test cavity is fully matched with the customer's product, and rapid and sensitive testing.
