New advanced 0.01~0.999 film packaging COF GM-6 coefficient of friction tester GM-6

The coefficient of friction tester is used to test the coefficient of frictionof plastic film, thin sheet, paper and so on, widely used in packaging industry, film-making companies and packaging material inspection agencies.

GM-F1 Inclined Coefficient of Friction Tester is expert applicable to the resolve of stationary coefficients of paper board, friction of paper, sheets, plastic films, convey belts and additional substances. By challenging the frictional possessions of substances, the open presentation of packages, packing rapidity of packers and additional indexes could be regulated to meet necessities for production.Different functions from other coefficient friction testers  (cof)    

  The coefficient of friction tester GM-4 is a measuring instrument developed and manufactured by the Guangzhou Biaoji R&D team based on various test standards of GB, ISO, ASTM and market demand. The measured friction coefficient determines the smoothness and opening difficulty of the film. and uniformity can be accurately determined, so as to correctly guide the production. It is suitable for measuring the static friction coefficient, dynamic friction coefficient and peel strength of plastic films, composite films, aluminum foils, aluminized films, plates, rubber, ceramics and other materials when sliding.        

GBDA-120 Compost Degradation Tester is designed in full compliance with standards such as ISO14855-1 and ASTM D5338. The mass of carbon dioxide released during biodegradation can be detected automatically, and the biodegradation percentage of degradable materials can be determined.  

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

N500 Gas Permeability Analyzer to test the gas (O2, N2, CO2 etc) transmission rate (GTR) of packaging materials, films and sheets materials

1 Function Ozone in the atmosphere is very little, while it’s a major factor in rubber cracking, the product simulate and enhance atmospheric ozone condition to study the role of ozone on the rubber, and to rapid identificate and evaluate rubber resistance for ozone aging and anti-ozone agent protection. According to“GB / T7762-2003 Test Method for Static Tensile Test of Ozone Resistance Cured Rubber or Thermoplastic Rubber”,“GB / T2951.21-2008 General Test Method for Insulation and Sheathing Material of Cable”,“GB / T 11206-2009 Rubber Aging test surface cracking method”, and other relevant standards of the test method. 2.1 Structure  All-in-one machine 2.2 Material a) Inner chamber: SUS304 stainless steel plate b) External chamber: SUS304 stainless steel plate or baking finish. Insulation: rigid polyurethane foam + aluminum insulation cotton with double protection. 2.3 Machine door a) Single door, open from left. b) Window frame / door frame with two silicone rubber seal and anti-condensation heating device. c)With observation window (W220xH250mm), lights above the window and door.  2.4 Requirements for sample holder (for dynamic-type only)       a)At both ends of the sample to be fixed with a clamp under the required elongation, the longitudinal direction of the specimen shall be substantially parallel to the direction of air flow when in contact with ozonized air. b) Clamps shall be made of a material (eg aluminum) which does not readily decompose ozone. c) Allow the sample to rotate at a speed between (20 ^ -25) mm / s, in a plane perpendicular to the dry gas flow, with each sample moving continuously along the same path. d) The time of one revolution of the same specimen is (8 ^ -12) min. The scanning area of the specimen shall be at least 40% of the effective area of the test chamber. Specimen preparation shall conform to the provisions of GB / T 9865.1. The test specimen is preferably cut from the new test piece and, if desired, may be cut from the finished product. At least 3 specimens shall be required for per test condition. The standard length of the specimen is not less than 10mm, and thickness not less than 0.2mm. The length of specimen between the two ends of the clamp before drawing is not less than 40mm. 3 Control panel a) Controller display b) Power switch c) Fault alarm d)Wavelength switch e)light switch button 4 Enclosure configuration a) With a stainless steel SUS # 304 shelf turntable b) One φ50mm lead hole:, and with a hole cover and silicone rubber plug. c) Move casters 4 pcs d) Horizontal mounting brackets 4 pcs e) There is a drainage hole in the back of the machine to facilitate the drainage of condensate; (8mm in diameter) Three-phase five-wire cable (four-core cable + protective grounding wire) 1 pc, (three meters long).

Medical Mask Exhalation Valve Air Tightness Tester  is Used to detect the air tightness of the mask breath valve. GBPI offers mask testing machines for surgical face masks, N95 masks, Melt-blown fabric. BFE Tester, PFE Tester, N95 Tester, Melt-blown fabric Tester      

It is used to test the percentage of materials containing bacteria suspended particles at the specified flow rate.

OTH-150DJ is used to test the performance of materials in various environments and test the heat resistance, cold resistance, dry resistance and humidity resistance of various materials. It is suitable for quality testing of products such as electronics, electrical appliances, mobile phones, communications, instruments, vehicles, plastic products, metals, food, chemicals, building materials, medical care, and aerospace.  

GBPI Melt Flow Indexer is a high prcise melt testing instruments for the measurement of thermoplastic melt flow rate(MFR) in quality control and research applications. It is suitable to meassure meltg flow charactor of PP,PE,POM, AR,PC,ABS plastic and plastic productions, widely used in plastic raw materials production, petrochemcial industry, scientific research departments and commodity inspection department.

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