It is suitable for sealing integrity testing ofpharmaceutical packaging to prevent moisture, oxygen, and microorganisms from contaminating products. Medicines: bottled, bagged, boxed, ampoules, vials, cartridges, prefilled needles (PFS), (BFS), (FFS), etc.
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 oftest 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.
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 |
1.5μm |
Display method |
10-inch touch color touch screen |
Voltage |
AC100V-240V, 50/60Hz, power ≤200W |
Weight |
Host: 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 |
Spray cans: plunger spray cans; bag-lined spray cans; "energy jacket" spray cans; flexible tube spray cans.
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