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Integrity Tests for Pharmaceutical Packaging Bottle Seal Liners

Integrity Tests for Pharmaceutical Packaging Bottle Seal Liners

50000 USD ($)/Set

Product Details:

  • Frequency 50/60 Hz
  • Features Non-destructive, fast analysis, high precision
  • Port Size 6 mm standard pneumatic connector
  • Gas Pressure 0.4~0.7 MPa
  • Hardness Applicable to soft and rigid liners
  • Application Pharmaceutical bottle seal integrity testing
  • Mounting Type Benchtop
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Integrity Tests for Pharmaceutical Packaging Bottle Seal Liners Price And Quantity

  • 1 Set
  • 50000 USD ($)/Set
  • 50000.00 - 100000.00 USD ($)/Set

Integrity Tests for Pharmaceutical Packaging Bottle Seal Liners Product Specifications

  • Seal liner integrity test
  • Benchtop
  • 0.5% F.S.
  • 0~50 N
  • 0~50 N
  • Non-destructive, fast analysis, high precision
  • 0~350 mm
  • 50/60 Hz
  • 6 mm standard pneumatic connector
  • Applicable to soft and rigid liners
  • 0.4~0.7 MPa
  • up to 300 mm
  • Pharmaceutical bottle seal integrity testing
  • Microcomputer controlled
  • 220V AC
  • 350 mm
  • 5~500 mm/min (adjustable)
  • 35 kg
  • Diameter up to 100 mm
  • 1s
  • Automatic
  • 20%~70% RH
  • RS232/USB
  • AC 220V, 50Hz
  • LCD digital display
  • Integrity Test System
  • 1~5 (Simultaneous Testing)
  • 0.01 N
  • 50 N load cell
  • 15C~40C

Product Description

Featuresnote1

Batch Testing

  • Equipped with fully-automatic gravity fed sample feeder, which is Labthinks latest scientific and technological achievement that can facilitate continuous testing of 20 to 120 samples.
  • A & B dual-channel design can test samples of two different specifications simultaneously.
  • The target vacuum degree can be set by the operator to meet testing requirements of different samples.
  • Dual methods of vacuum decay and pressure decay provide the flexibility to accommodate various types of package samples.

Precise Data

  • Advanced pressure detection technology, using world renowned components for data stability which is not affected by ambient environment.
  • Advanced microflow automatic flow control technology that can accurately simulate different sizes of leakage holes without manual adjustment.
  • Both the differential pressure transducer and flow meter are traceable to NIST.
  • The system can achieve a higher test repeatability of 1um.

Intelligent Control

  • 15.6" embedded touch tablet computer with Windows OS.
  • New longitudinal interface layout, and easy to use graphic user interface.
  • Automatic alarm, automatic capture, automatic collection of unqualified samples.
  • The pressure curve is displayed in real time, and the test results are counted automatically.
  • Leakage rates are calculated automatically.
  • The system is equipped with various sensors as intelligent reminders for safer operation and control.
  • Universal printer can be connected for test results output.
  • The system features embedded with USB and network ports to facilitate the external access and data transmission of the system, which can be upgraded remotely

Security Compliance

  • Verified by compensation and calibration methods.
  • The leak tester meets GMP requirements for data traceability and meets the needs of the pharmaceutical industry.
  • User operation permission is managed at multiple levels, and the permission content can be configured on demand.
  • Electronic signature is designed according to the standard requirements of 21 CFR Part11.

Test Principle

The sample is placed in the sample feeder and automatically delivered into the test cell. The leak rate and other results can be calculated and obtained by analyzing pressure changes measured by the sensor.

Reference Standards

ASTM F2338, YY-T 0681.18, and USP<1207>

Applications

Basic Applications Vials Various vial sealing test.
Extended Applications Ampoule Various ampoule bottle sealing tests.
Cartridge Bottles Various cartridge bottle sealing tests.
Injection bottles Various injection bottles sealing test.

Technical Parameters

Table 1: Test Parameters Note2

ParameterModel C690H
Testing Range um(Reference aperture size USP1207) 3i8igreat leakage
Detection Lower Limit um 3
Resolution um 0.1
Repeatability um 1
Pressure Range kPa -100i0ii14100
Extended Functions 21 CFR Part11 Optional
GMP computer system requirements Optional

Table 2: Technical Specifications

Testing Cell 1 set for A group and 1 set for B group
Sample Feeder 1 set for A group and 1 set for B group
Sample Size I45 mm80mmNote3
Sample Quantity 20120 pieces
Gas Specifications Compressed Air (Gas source is provided by the user)
Gas Source Pressure 40.6 PSI / 500 kPa
Port Size I6 mm Polyurethane tube
Dimensions 33.4 H x 19.6 W x 28.7 D (85cm 50cm 73cm)
Power 120VAC10% 60Hz / 220VAC10% 50Hzi14select one from the twoi14
Net weight 209Lbs (95kg)

Product Configuration

Standard Configuration Mainframe, embedded tablet computer, software, flow meter, European vacuum pump, I6 mm polyurethane tube
Customization Test cell and sample feeder of group A, test cell and sample feeder of group B, negative standard reference sample and positive standard reference sample designed according to sample specifications
Optional Parts GMP computer system requirements, 21 CFR Part11, air compressor, IQ/OQ/PQ documents

Note 1: The described product characteristics are subject to the specific annotation of the "Technical Parameters" table.
Note 2: The parameters in the table are measured in the Labthink laboratory by professional operators according to the requirements and conditions of the relevant laboratory environmental standards.
Note 3: Group C test cell can be customized for samples beyond the "Sample Size", but the lower detection limit and test range will change according to the sample size, and the actual delivery shall prevail.



Regulatory-Compliant Testing

Designed specifically for pharmaceutical applications, the system complies with USP and FDA standards, ensuring your bottle seal integrity processes meet stringent regulatory guidelines. This compliance supports product safety and strengthens confidence in your packaging solutions.


Advanced Test Methods and Data Management

Featuring state-of-the-art vacuum decay and pressure hold testing, the equipment provides pass/fail verdicts with numeric leak data for detailed analysis. It includes microcomputer controls, LCD digital display, and stores over 500 test results, streamlining quality control workflows and traceability.


Flexible and Efficient Testing Framework

Adapting to a wide range of liner materials-induction, pressure sensitive, or foam-the system enables concurrent testing of up to five specimens. Adjustable parameters, fast analysis times, and a non-destructive approach optimize testing efficiency without compromising sample quality.

FAQ's of Integrity Tests for Pharmaceutical Packaging Bottle Seal Liners:


Q: How does the Integrity Test System detect seal liner leaks in pharmaceutical bottles?

A: The system employs vacuum decay and pressure hold methods to identify leaks in the seal liners of pharmaceutical packaging. It creates a controlled pressure environment around the sample and monitors pressure changes to indicate leakage, providing both pass/fail results and precise numeric data.

Q: What types of seal liners are compatible with this test method?

A: The device is compatible with various seal liner types, including induction, pressure sensitive, and foam liners. Its flexible clamping and adjustable testing parameters allow it to evaluate both soft and rigid liners, making it suitable for a broad spectrum of pharmaceutical applications.

Q: When should pharmaceutical companies use this Integrity Test System?

A: Pharmaceutical manufacturers and quality assurance labs should use this system during routine quality control inspections, process validation, and prior to product release. It ensures packaging integrity to maintain sterility and regulatory compliance throughout the product lifecycle.

Q: Where can I access technical support for the Integrity Test System?

A: Technical support is available both online and onsite. As an exporter, manufacturer, and supplier based in China, we provide responsive service support to address user inquiries, perform maintenance, or resolve technical issues efficiently.

Q: What is the process for conducting an integrity test with this machine?

A: To perform a test, mount up to five bottles (with seal liners) onto the benchtop system. Set test parameters via the microcomputer control panel, initiate the test, and the device will automatically carry out the vacuum decay or pressure hold method. Results are displayed on the LCD screen and saved for record-keeping.

Q: What are the main benefits of using this Integrity Test System?

A: Key advantages include non-destructive, fast, and accurate testing; simultaneous multi-specimen analysis; regulatory compliance; numeric leak quantification; and robust overload protection. This enhances operational efficiency, supports data-driven quality assurance, and minimizes sample wastage.

Q: How are the test results stored and managed?

A: The system can store over 500 test results in its internal memory, with options to export data via RS232 or USB interfaces. Results include pass/fail status and detailed leak measurements, facilitating easy traceability and audit readiness for pharmaceutical companies.

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