Flexible Packaging Film Coefficient of Friction Tester COF Testing

Heat Seal Tester apply to test the temperature, pressure, time and strength for heat sealing of various plastic films, composite film, aluminum foil and so on, widely used in industries of , food, pharmaceuticals, inspection agency, research institute and so on.

GBPI offers mask testing machines for surgical face masks, N95 masks, Melt-blown fabric. BFE Tester, PFE Tester, N95 Tester, Melt-blown fabric Tester

Product Brief The N600C Carbon Paper Air Permeability Rate Tester is designed and developed in accordance with GB/T 20042.7-2014. Adopting the differential pressure method as its testing principle, it is professionally used for measuring the air permeability rate of various types of carbon paper for proton exchange membrane fuel cells (PEMFC). Testing Principle Based on the differential pressure method, the sample is placed between two fixtures, forming a constant differential pressure on both sides of the sample. Driven by the differential pressure, gas flows from the high-pressure side through the sample to the low-pressure side. The air permeability rate of the carbon paper is calculated based on the transmission flow rate, sample thickness, test area, and test differential pressure. Executed Standards GB/T 20042.7-2014 Technical Parameters Item Technical Parameters Test Range 0~200,000 mL·mm/(cm²·h·mmHg)0~14,701 mL·mm/(cm²·hr·mmAq) Resolution 0.1 mL·mm/(cm²·h·mmHg)0.1 mL·mm/(cm²·hr·mmAq) Pressure Range 0~500 Pa (other ranges available upon request) Pressure Resolution 0.1 Pa Pressure Accuracy 0.1% FS (Full Scale) Flow Range 0~50 L/min (other ranges available upon request) Flow Resolution 1 mL/min Flow Accuracy 1% FS (Full Scale) Test Area 16 cm² Instrument Dimensions 410 mm×295 mm×365 mm Power 100 W Power Supply 110~250 VAC, 50~60 Hz Product Features • The instrument's differential pressure is adjustable within the range of 0~500 Pa, with an accuracy of 0.1% FS, fully meeting the test pressure requirements of different samples;• The test range can be customized according to different sample requirements;• Arbitrary pressure adjustment, fully automatic operation, and automatic measurement and calculation of results;• Equipped with a color touch screen, no external computer required;• Built-in micro-printer for real-time printing of test reports;• The upper computer software is designed in accordance with the new GMP Appendix "Computerized Systems", supporting functions such as hierarchical permission management, audit trail, and electronic signature (optional).  

Used for face mask air flow resistance and differential pressure testing to check breathability and can also be used to check differential pressure of textile materials gas exchanger.

Vertical Counter‑Pressure Retort LS‑35L/50L/75L/100L | Dual‑Mode Sterilization for Food Packaging Aseptic Testing LS‑series Vertical Counter‑Pressure Retort for Food Packaging Sterilization & Laboratory Aseptic Validation Product Introduction Reliable dual‑mode counter‑pressure sterilizer tailored for food packaging quality control & lab aseptic evaluation. The vertical counter‑pressure retort is a medium‑small‑size mechanically program‑controlled counter‑pressure sterilization equipment. The sterilizer adopts electric heating mode. Water is directly injected into the sterilizing chamber and heated to generate high‑pressure steam required for sterilization to disinfect articles. After sterilization is completed, external compressed air and water pressure are applied for rapid cooling within 3 minutes, cooling internal articles down to 30‑40℃. Equipped with program control, it supports two operation modes: boiling disinfection and pressure sterilization with rapid cooling. Boiling temperature can be set ≤100℃. The rapid‑cooling pressure sterilization temperature is pre‑selectable within 101℃‑135℃. It is integrated with heater overload protection and buzzer alarm upon sterilization completion. Featuring simple operation and high safety reliability. This unit is suitable for disinfection and sterilization of food packaging, utensils and instruments. It is an ideal device especially for aseptic tests in food research institutions. Working Principle Dual‑sterilization logic enables boiling disinfection & high‑pressure counter‑pressure sterilization, simulating real‑world thermal processing conditions for flexible packaging samples. This equipment is designed with two disinfection & sterilization principles to deliver dual‑function performance for customers. The heater directly heats water to produce pressurized steam. The pressurized steam acts on microorganisms on samples and destroys their structures to realize sterilization. When rapid‑cooling sterilization program starts, 6 liters of tap water is first injected into the chamber. After around 25‑minute heating process, it enters sterilization holding stage with sterilization duration of 35‑40 minutes. When sterilization finishes, 0.24 MPa compressed air and tap‑water pressure are manually fed into the chamber, then half‑open the drain valve to discharge water and implement counter‑pressure cooling for flexible packages and other specimens. Rapid cooling lasts for 3 minutes. Manually cut‑off compressed air and tap‑water supply, and internal articles can be cooled down to 30‑40℃. Core Advantages Dual‑mode operation: boiling disinfection & counter‑pressure pressure sterilization Ultra‑fast 3‑minute counter‑pressure cooling to avoid flexible pouch deformation Heater overload protection & buzzer alarm when sterilization cycle completes Multiple chamber volume options:35L‑50L‑75L‑100L for different test throughput Mechanical program control, easy operation for laboratory staff Technical Parameters Item Specifications Max Working Pressure 0.22 MPa (30 Psi) Max Working Temperature 135℃ Sterilization Temperature Selection 101‑135℃ Boiling Temperature Selection ≤100℃ Timer Range 1‑60 min Effective Chamber Volume 35L, 50L, 75L, 100L Power / Power Supply 2.5 KW / AC220V, 50Hz; 3 KW / AC220V, 50Hz; 4.5 KW / AC220V, 50Hz Overall Dimension 570×550×970 mm(35L);590×590×1110 mm(50L);650×630×1150 mm(75L);680×650×1220 mm(100L) Gross / Net Weight 56/42 kg(35L); 68/50 kg(50L); 90/70 kg(75L); 105/85 kg(100L) Application Scenarios Widely adopted in food R&D laboratories, packaging manufacturers and quality inspection institutes for sterilization and thermal‑resistance assessment of flexible food packaging materials. Disinfection & sterilization for food flexible packaging, containers and lab utensils Aseptic test and thermal resistance evaluation for food packaging samples Sterilization for laboratory instruments and small‑batch food test specimens Get Custom Solution & Quotation GBPI Packaging Test EquipmentOfficial Website: www.gbpitester.com

Face Mask Particulate Filtration Efficiency is to test the filtering efficiency of particulate protective masks . This instrument conforms to ASTM F2299, NIOSH-42CFR-84, GB 2626-2019, YY 0469-2011 and GB/T32610-2016 standard. GBPI offers mask testing machines for surgical face masks, N95 masks, Melt-blown fabric. BFE Tester, PFE Tester, N95 Tester, Melt-blown fabric Tester.

Electronic Leakage Tester applies to test the hermetic sealing quality and performance of packaging bags, bottles, cans and so on, used in industries of food, beverage, pharmaceuticals, personal care and so on          

AUTO GBM‑L2 Dual‑Pressure Micro‑Leak Seal Tester: Micro‑Leakage Detection for Pharmaceutical & Food Packaging GBPI AUTO GBM‑L2 Dual‑Pressure Micro‑Leak Seal Tester for Packaging Micro‑Leak Detection Product Introduction AUTO GBM‑L2 Dual‑Pressure Methods Vacuum Decay Leak Detection Tester adopts the test principle of vacuum decay method/pressure decay to detect micro‑leakage of finished packaging. It can be applied to packaging systems composed of vials, ampoules, pre‑filled syringes, eye drop bottles, HDPE bottles, infusion bottles/bags and other pharmaceutical packaging, food packaging, and chemical industry packaging. Testing Principle The host is connected to a sealed test chamber customized according to the sample. When performing the vacuum decay method test, the instrument evacuates the test chamber, and a pressure difference is formed inside and outside the sample. Under the action of the pressure, the gas/liquid in the sample enters the test chamber through the leak hole. The main engine uses the absolute pressure sensor and the differential pressure sensor to monitor the pressure change in the chamber to judge whether the sample leaks. When performing the pressure decay method test, the instrument fills the test chamber with a predetermined air pressure, and the gas in the test chamber enters the sample through the leak hole. The host uses absolute pressure sensors and differential pressure sensors to monitor the pressure changes in the chamber to determine whether the sample is leaking. Executive Standards ASTM F2338‑2009(2013), YY‑T 0681.18‑2020, USP<1207.2>, ASTM F2095, supporting leakage verification for global pharmaceutical and food packaging regulatory requirements. Core Technical Parameters Absolute Pressure Testing Range (0‑300) kPa Differential Pressure Testing Range (-2‑2) kPa Detection Sensitivity 1‑3 μm Balancing / Testing Time 1‑3600 s Vacuum Purge Time 1‑3600 s Set Flow Rate 0‑3 mL/min Testing System Dual Sensor Technology / Dual Cycle Testing Testing Chamber Customized according to the sample Applicable Products Vials, Ampoules, Prefilled Syringes, Infusion Bottles/Bags, etc. Detection Principle Vacuum Decay Method / Pressure Decay Method Dimensions of the Main Unit 495 mm*455 mm*280 mm Ambient Temperature 20℃‑25℃ Relative Humidity 40%‑60% Working Power Supply AC 220V, 50HZ Product Features • Dual‑Pressure Methods, to help solve testing difficulties. The double combination of vacuum decay method and pressure decay method solves the problem of easy misjudgment and false negative for freeze‑dried powder injections containing vacuum in the bottle using a single vacuum decay method. Based on dual‑sensor and dual‑circulation system technology, high‑quality absolute pressure sensor and differential pressure sensor, with an accuracy of 0.1% FS, can effectively detect large and small leaks, accurately calculate the leak hole diameter, and give a pass or fail judgment. • Low detection sensitivity and good test repeatability. For rigid samples, the detection sensitivity is as low as 1 μm, and the test repeatability is as low as 0.8%. The instrument has stable performance, low noise and good repeatability. • Imported brand accessories, excellent performance. Imported brand vacuum pump, pumping rate up to 3 L/s, noise as low as 50 DB, high ultimate vacuum, convenient oil level detection and replacement. The imported gas mass flow controller can simulate micro‑leaks arbitrarily, with a resolution of 0.001 mL/min, which provides a reliable guarantee for the method verification of instrument sensitivity. • Large‑size touch screen, intelligent operation. Color 7‑inch touch screen, clear view, sensitive touch, easy to operate. Equipped with a micro‑printer, USB data interface, and supports PC software measurement and control operation. The test software is designed according to the GMP appendix "Computerized System". It has an audit trail function and multi‑level authority settings for users, which can meet the needs of the pharmaceutical industry for data traceability. • Personalized customization to meet the needs of different samples. For different test samples, it supports customization of suitable test chambers to meet the needs of different tests. For the same type of samples, it supports customized nesting mode, which can realize the sharing of a test chamber for samples of various specifications. Application Fields Freeze‑dried powder injection Injection Prefill needle Eye drops Plastic Ampoule BFS Infusion bags Factory Configuration Standard Host machine, vacuum pump, test chamber and 3 sets of yin and yang control (customized as required), 11‑inch touch panel, professional software (GMP) Optional Imported gas flow meters, air compressors, printers, calibration certificates Conclusion AUTO GBM‑L2 dual‑pressure micro‑leak seal tester combines vacuum‑decay and pressure‑decay technology, solving false‑negative defects existing in single‑mode leak detection for vacuum‑containing pharmaceutical containers. With imported core components, audit‑trail data function and customizable test chamber, it is ideal micro‑leakage inspection equipment for pharmaceutical factories, third‑party testing laboratories and R&D institutions for parenteral preparation packaging quality control. Get Quotation for This Unit GBPI Packaging Test Equipment ManufacturerAddress: No.3 Linjiang Road, Xiagang Subdistrict, Huangpu District, Guangzhou, Guangdong, ChinaTel: +86 15820231129 | Official Website: www.gbpitester.com

The identification and quantitation of residual printing solvents in synthetic packaging materials are very important for the material packaging suppliers, the printers and the packaging users of food and pharmaceutical products.

Torque tester HP-200 is a testing instrument for bottle cap locking and opening based on ASTM and GB standard requirements and market demand developed and manufactured by GBPI R&D team. For bottle packaging products, nozzle packaging products and tube packaging products, the size of the cap opening torque is one of the key control parameters, which has a great impact on the intermediate transportation and final consumption of the product.It is suitable for measuring the size of the locking and opening torque of bottle products, and is an indispensable test equipment in the production process.

Didital thickness tester is used to make thickness measuring or comparative measuring of plastic film, thin sheet, paper and so on.

The torque tester is professionally suitable for testing the torque value of the caps of packaging products such as bottles, beverage bottles, mineral water bottles, and milk bottles. It is an ideal configuration instrument for offline or online testing of production units in the packaging industry.