It 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.
Pharmaceutical industry
Medical device industry
Food and beverage industry
- ◆ Differential pressure sensor±2kpa, error≤0.5%F.S.
- ◆ Differential pressure resolution0.1pa
- ◆ Test pressure sensorError≤±1%F.S.
- ◆ Test pressure range-0.1～0.2Mpa /-0.1～0.7MPa/-0.1～1.0Mpa（operational）
- ◆ Minimum detectable aperture2μm ( for IV bag minimum 5μm)
- ◆ Display method10-inch touch color touch screen
- ◆ VoltageAC100V-240V, 50/60Hz, power ≤200W
- ◆ Audit trail>=5 years of storage Multiple event logs, which can be queried according to time
- ◆ Authority managementLogin with username and password, level 4 authority, meet FDA 21CFR PART 11 requirements
- ◆ Print functionBuilt in printer
- ◆ History record>=300000 storage
- ◆ Data backupSupport U disk to export data
- ◆ InterfaceEthernet USB RS485(operational)
Packaging Leak Tester
MFT-800
1. 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 ,pressure decay 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.
2. Advantage function:
◎Adpot automous optimization Linux system
◎Automatically test the flow rate and change the aperture size during the whole process.
◎Automatic leak flow calibration function.
◎Equipped with standard leaks (standard leak 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(mould) 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.
