Packaging Leak Tester MFT-1000

Packaging Leak Tester MFT-1000

Negotiable /Set

Min.Order:1 Set

Supply Ability:
200 Set / Sets per Month
Port:
Beijing
Payment Terms:
T/T L/C D/P D/A Credit Card PayPal Cash Escrow Other
Delivery Detail:
2 days

Quick Details View All >

Brand Name:
Beijing Neruonbc
Place of Origin:
China
Model Number:
MFT-1000

Beijing Neuronbc Laboratories Co.,Ltd.

Business license
Business Type: Manufacturer
Main Products: filter integrity tester ,TOC analyzer ,Glove integrity tester ,Packaging leak tester ,wireless glove integrity tester ,Freezing point osmometer

Product Details

Packaging Leak Tester

MFT-1000

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.

 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.

 

 3. Specifications:

Differential   pressure sensor

±2kpa,   error≤0.5%F.S.

Differential   pressure resolution

0.1pa

Test pressure   sensor

Error≤±1%F.S.

Test pressure   range

-0.10.2Mpa /-0.10.7MPa/-0.11.0Mpaoperational

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(operational)

 


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