MFT-1000

Description :

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.

With audit trail function.
Automatic leak flow calibration function.
Four-level user authority management meets FDA 21CFR PART 11 requirements.
plit 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.

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Parameters

Dimensions	430655420*330
Weighing	51kg
Measurement Methods	Vacuum attenuation method、Pressure attenuation method
Power Supply	100-240VAC 50-60Hz
Differential Pressure sensor	-2~2kpa/ error≤0.5% F.S
Differential Pressure resolution	0.1pa/0.01pa
Test Sensitivity	0.00057sccm
Pressure test range	-0.1~0.2Mpa
	-0.1~0.7Mpa
	-0.1~1.0Mpa
Minimum detectable aperture	1.5μm
Export Data	Yes(USB)
Historical Records	≥5 years
Audit Trail	≥5 years storage multiple event logs can be queried according to time
Print Function	Built-in niddle printer
Signal output	4-20mA, RS485,12V alarm output
GMP quality	Yes
Communication interface	Ethernet USB RS485

MFT-1000

Parameters

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