Packaging Testing Instruments

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. Spray cans: plunger spray cans; bag-lined spray cans; "energy jacket" spray cans; flexible tube spray cans.(video is MFT-600)if need others contact me pls.

packaging testing instruments

MOdel: MFT-1000

Parameters:

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(optional)
Minimum detectable aperture	2μm ( for IV bag minimum 5μm)
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	Built in printer
History record	>=300000 storage
Data backup	Support U disk to export data
Interface	Ethernet USB RS485(optional)

Main 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.

● 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.

Packaging testing instruments 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.

Application: