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Enhancing Pharmaceutical Packaging Performance by Detailed Analysis of Vacuum Pressure Decay

Enhancing Pharmaceutical Packaging Performance by Detailed Analysis of Vacuum Pressure Decay

50000 USD ($)/Set

Product Details:

  • Test Range 0 to -90 kPa
  • Specimen Size Up to 300 mm (custom sizes supported)
  • Sensor High-precision pressure transducer
  • Accuracy 0.5% F.S.
  • Humidity 85% RH
  • Test Material Pharmaceutical packaging (vials, blisters, bottles)
  • Response Time 1 second
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Enhancing Pharmaceutical Packaging Performance by Detailed Analysis of Vacuum Pressure Decay Price And Quantity

  • 50000.00 - 500000.00 USD ($)/Set
  • 50000 USD ($)/Set
  • 1 Set

Enhancing Pharmaceutical Packaging Performance by Detailed Analysis of Vacuum Pressure Decay Product Specifications

  • High-precision pressure transducer
  • 0 to -90 kPa
  • Up to 300 mm (custom sizes supported)
  • 0.5% F.S.
  • 85% RH
  • 6 mm
  • Pharmaceutical packaging (vials, blisters, bottles)
  • Vacuum Leak Detector
  • Air
  • Vacuum Pressure Decay Analysis
  • Pharmaceutical Packaging Integrity Testing
  • Standard (Customizable on request)
  • 1 second
  • 18 kg
  • Room temperature (10C to 40C)
  • Stainless Steel
  • Digital LCD touch screen
  • 220V AC, 50Hz
  • Single phase, 220V AC
  • Adjustable, according to standard requirements
  • Up to 4 at once
  • 10C to 40C

Enhancing Pharmaceutical Packaging Performance by Detailed Analysis of Vacuum Pressure Decay Trade Information

  • 1 Set Per Week
  • 1 Week
  • Yes
  • Contact us for information regarding our sample policy
  • Asia, Australia, Central America, North America, South America, Eastern Europe, Western Europe, Middle East, Africa

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.



Microprocessor-Controlled Accuracy for Reliable Results

Engineered to uphold the highest industry standards, this vacuum leak detector utilizes advanced microprocessor controls. Automatic and manual calibration ensure consistent measurements, while a high-precision pressure transducer supports an accuracy of 0.5% F.S. The digital LCD touch screen makes operation and data review intuitive. Laboratories benefit from reproducible results that foster compliance and data-driven quality assurance.


Safe, Flexible Testing for Today's Packaging Challenges

Featuring over-pressure protection, emergency stop, and compliance with CE and ISO 9001, this system ensures a safe and user-friendly experience. Adjustable parameters such as gas pressure, test cycle duration, and specimen size (up to 300 mm) make it versatile for a variety of pharmaceutical packaging types-vials, blisters, and bottles. The robust stainless-steel construction guarantees durability in demanding lab environments.


Comprehensive Data Management and Export Capability

Efficient data management is vital. The system outputs detailed test results through USB and RS232 ports for easy integration into LIMS or QA systems. Users can export and analyze results to enhance process control, track batch performance, and compile compliance reports. These features streamline regulatory audits and perennial improvements in packaging quality.

FAQ's of Enhancing Pharmaceutical Packaging Performance by Detailed Analysis of Vacuum Pressure Decay:


Q: How does the vacuum leak detector analyze pharmaceutical packaging integrity?

A: The vacuum leak detector uses a vacuum pressure decay method to assess the integrity of pharmaceutical packaging. By creating a controlled vacuum environment within the 10-liter chamber, it identifies leaks based on any pressure change, delivering precise measurements using a high-precision transducer. Tests run automatically for cycles adjustable from 30 seconds up to 5 minutes.

Q: What types of packaging and specimen sizes can the system test?

A: The device is engineered to test pharmaceutical packaging such as vials, blisters, and bottles. It supports specimens up to 300 mm, with customizable options available to accommodate larger or specialized packaging formats if needed.

Q: When should I use automatic versus manual calibration modes?

A: Automatic calibration is ideal for routine quality checks to maintain consistent accuracy with minimal intervention. Manual calibration can be employed when adapting to new test methods, investigating anomalies, or adjusting for specific packaging types, ensuring maximum flexibility and reliability.

Q: Where can I access data outputs, and how is test data managed?

A: Test data can be exported via convenient USB or RS232 connections, enabling seamless integration with laboratory information management systems or for immediate reporting. This supports efficient tracking, compliance documentation, and in-depth quality assessments.

Q: What is the typical process for conducting a test with this vacuum leak detector?

A: To perform a test, place up to four packages in the chamber, select desired settings (pressure, duration), and start the process via the LCD touch screen. The microprocessor handles test execution and data collection, while alarms alert users to any detected leaks. Results appear digitally for review or export.

Q: How does this system benefit pharmaceutical manufacturers and exporters?

A: Manufacturers benefit from enhanced quality assurance, reduced product recalls, and simplified compliance with USP <1207> and ASTM F2338 standards. The system's fast response, data traceability, and robust safety features support efficient operation and regulatory readiness, vital for both domestic and international markets.

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