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Product description
• Tested to EN374
• Tested to ASTM D6978-05
• Extended cuff (300mm glove length)
• AQL 0.65 and EN455 parts 1-4
• Free from latex
• Free from powder
• Free from phthalates
• Tested to EN1186
• Ambidextrous
• Manufactured using high-quality nitrile
• Nitrile formulation conforms to the hand during use
• Beaded cuff
• Manufactured with textured palms and fingers
• Heavy-weight construction
• Touchscreen compatible
Fingertips refer to the tips of the fingers, it also can refer to the reinforcement on gloves or other garments to protect the fingertips. The requirements for fingertips vary depending on the intended use and the environmental conditions. Fingertips reinforcement will provide more protection from abrasion and impact, while a thinner fingertips will be more flexible and easier to move in. Different types of gloves or other garments may have different requirements for fingertips, such as a work gloves that need to be reinforced for protection or a gloves that need to be flexible for dexterity. It's important to choose the right fingertip design that meets the specific needs and requirements of the intended use and environment.
Ambidextrous refers to the ability to use both hands equally well. It can be used to describe people or things that are able to perform tasks equally well with either hand. For people, ambidexterity is not something that can be acquired, it is something that is inherent, meaning it's a natural ability or trait. However, some people may develop ambidexterity through practice and training. Ambidexterity is not a requirement for most tasks, but it can be beneficial in certain activities such as playing sports or playing musical instruments.
Full finger refers to a type of glove or mitten that covers the entire finger, including the tip. It is designed to protect the fingers from cold weather, injuries, or other hazards. The requirements for what is considered a "full finger" glove or mitten can vary depending on the context, but generally it should cover the entire finger including the tip, providing protection to the entire finger.
"Chlorinated" refers to something that has been treated with chlorine, a chemical element that can be used as a disinfectant or bleach. The requirements for something being chlorinated will vary depending on the specific application or use. It may require a certain amount of chlorine to be used or a specific amount of time for the chlorine to be in contact with the material. Chlorination process should be done in accordance with the safety guidelines and regulations.
A touch screen is a type of display screen that can sense the touch of a finger or other object. It's a input device that you can use to interact with electronic devices like smartphones, tablets, laptops, and more. It works by detecting the touch of a finger or stylus and converting it into an electronic signal that the device can understand. The requirements for a touch screen can vary depending on the specific application, but it should be responsive and accurate in detecting touch inputs. They can be made with different technology like capacitive, resistive or infrared.
Multi-purpose refers to something that can be used for multiple purposes or functions, instead of being designed for just one. An example of a multi-purpose item is a tool that can be used for different types of tasks, such as a swiss army knife that can be used as a knife, a can opener, and a screwdriver. The requirements for a multi-purpose item are that it should be able to perform multiple functions effectively, be durable, and easy to use. It should also be versatile, able to adapt to different needs, and have a good performance. Additionally, it should be safe and reliable.
"Latex free" means that a product does not contain latex, a type of rubber that can cause allergic reactions in some people. The requirement for a product to be labeled as "latex free" is that it must not contain any latex. This is important for products such as gloves that come into contact with skin or medical equipment that come into contact with mucous membranes.
A long sleeve is a type of clothing that covers the arms from the wrist to the shoulder. The requirements for a long sleeve shirt or garment would vary depending on the context, but it should have sleeves that are longer than the normal short sleeves. It can be made from different materials and can vary in style and design.
Phthalates are a group of chemicals commonly used in the production of plastic items such as toys, clothing, and personal care products. Phthalate-free refers to products that do not contain these chemicals. The requirements for phthalate-free products vary depending on the country or organization certifying them. Typically, they have to pass certain tests to ensure that they do not contain harmful levels of phthalates.
Powder is a dry substance that is made up of small particles. It can be made from different materials such as minerals, chemicals, or food. Powders can be used for various purposes such as in cosmetics, cleaning products, medication, and food ingredients. To be considered a powder, it should be a dry substance that is made up of small particles, it can be made from different materials, and it can be used for various purposes.
Color is a visual characteristic of objects, surfaces, or light that is determined by the way it reflects or emits light. Color can be described by its hue, saturation, and brightness. The requirements for what is considered a "color" can vary depending on the context, but generally it should be a visual characteristic of an object, surface, or light that is determined by the way it reflects or emits light.
A material is something that is made from different substances or elements, like wood, metal, plastic, or fabric. It can be used to make things like clothes, furniture, and buildings. Different materials have different properties and can be used for different purposes. Some materials are stronger than others, some are more flexible, and some are better at resisting heat or cold. Some are made from natural sources, while others are synthetic. The requirements for a material depend on the specific use it will be put to.
Cuff thickness refers to the thickness of the material used to make the cuff of a garment, such as a glove, a shirt, or a pants. The requirements for cuff thickness vary depending on the intended use and the environmental conditions. A thicker cuff will provide more insulation and protection from the elements, while a thinner cuff will be more flexible and easier to move in. Different types of garments may have different requirements for cuff thickness, such as a glove that needs to be flexible for dexterity or a jacket that needs to be insulated for warmth. It's important to choose the right cuff thickness that meets the specific needs and requirements of the intended use and environment.
Finger thickness refers to the thickness of the material used to make the fingers of a garment such as a glove. The requirements for finger thickness vary depending on the intended use and the environmental conditions. A thicker finger will provide more insulation and protection from the elements, while a thinner finger will be more flexible and easier to move in. Different types of gloves may have different requirements for finger thickness, such as a work gloves that need to be reinforced for protection or a gloves that need to be flexible for dexterity. It's important to choose the right finger thickness that meets the specific needs and requirements of the intended use and environment.
Length refers to the distance from one end to another end of an object or surface. It is a measure of the horizontal dimension of an object. The requirements for length will depend on the purpose of the object and the context in which it will be used. For example, the length of a room will be different than the length of a swimming pool and the length of a car will be different than the length of a book.
Palm thickness refers to the thickness of the material used to make the palm of a glove or other garment. The requirements for palm thickness vary depending on the intended use and the environmental conditions. A thicker palm will provide more insulation and protection from the elements, while a thinner palm will be more flexible and easier to move in. Different types of gloves or other garments may have different requirements for palm thickness, such as a work gloves that need to be reinforced for protection or gloves that need to be flexible for dexterity. It's important to choose the right palm thickness that meets the specific needs and requirements of the intended use and environment.
Shelf life is the length of time a product can be stored and still be safe to use or consume. It depends on the product and how it's stored. Some products have a short shelf life, like fresh food, while others have a long shelf life, like canned goods. It is important to check the expiration date and to properly store the product to ensure that it stays safe to use.
Weight is a measure of the force exerted on an object due to gravity. The weight of an object is determined by its mass and the acceleration due to gravity. The unit of weight is typically measured in pounds or kilograms. The requirements for weight can vary depending on the intended use of the object or material, but generally, it should be appropriate for the intended purpose and safe to handle. For example, a weight of a car part should be light enough to not affect the car's performance but strong enough to withstand the forces acting on it, and a weight of a packaging material should be able to hold the weight of the contents without breaking. Additionally, certain professions such as weightlifting, aviation or transportation have specific weight requirements to ensure safety and efficiency.
A surface is the outer layer of something. It can be the top layer of a solid object or the outer layer of a liquid or gas. The requirements of a surface can vary depending on its intended use. For example, a surface that will be walked on needs to be slip-resistant, and a surface that will be painted needs to be clean and smooth.
- Hand Protection
- Chemical Resistance
- Clean Room
- Food Service
- Medical Protection
- Antimicrobial Protection
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Standards and labels
EN 374-4:2013 is a European standard for gloves that protect against microorganisms. It sets rules for how the gloves should protect against microorganisms and how to test if they meet the standards. Gloves that pass the tests can have a label that says they meet the standard. The test results can be pass or fail for each test that checks the gloves resistance to microorganisms.
Test results
Degradation TestedThe standard EN 374-4:2013 pertains to the determination of degradation by chemicals for protective gloves. Degradation is assessed based on the change in physical properties of the glove material after contact with a chemical. Specifically, a result indicating degradation provides a measure of the glove's deterioration in terms of features like tensile strength and elongation when exposed to specific chemicals, gauged through physical tests such as elongation and tensile tests. The test method involves exposing the glove material to the chemical over a determined period, followed by mechanical testing to compare the pre and post-exposure properties. This result is crucial in determining the glove's suitability for use with specific chemicals, as degradation can significantly reduce its protective effectiveness, potentially endangering the user. Hence, understanding and adhering to this standard helps in the selection of appropriate protective gloves for specific chemical exposure scenarios, ensuring user safety and compliance with health and safety regulations.
EN ISO 374-1:2016 is a standard that defines the performance requirements for gloves that protect against chemicals and microorganisms. The standard specifies the design, materials, and testing requirements for gloves to protect against chemicals and microorganisms. Possible test results include measurements of the gloves' permeation resistance, degradation, and penetration. It also includes the safety and functionality requirements for gloves.
Test results
Specified Requirements Type CEN 374-5:2016 is a European standard for gloves that protect against microorganisms, specifically gloves that are used for medical and dental procedures. It sets rules for how the gloves should protect against microorganisms and how to test if they meet the standards. Gloves that pass the tests can have a label that says they meet the standard. The test results can be pass or fail for each test that checks the gloves resistance to microorganisms.
Test results
Micro-organisms Bacteria & FungiEN 374-5:2016 specifies the requirements and test methods for protective gloves intended to protect against bacteria and fungi. The designation 'Bacteria & Fungi' indicates that the gloves have been tested and verified to provide effective barrier protection against microbial agents. The testing involves evaluating the glove's material and seams for their impermeability to microorganisms under conditions that simulate real-world use, ensuring no penetration occurs through the glove material or at the seams. Gloves certified under this standard are crucial for use in environments such as healthcare, laboratory settings, and any applications where preventing the transmission of infectious agents is essential. They help ensure the safety and hygiene of workers by providing reliable protection against the risks of bacterial and fungal contamination.
Micro-organisms VirusEN 374-5:2016 is a standard that outlines the requirements and testing methods for protective gloves designed to protect against viruses. The designation 'Virus' indicates that the gloves have passed specific tests confirming their barrier effectiveness against viruses. These tests involve assessing the glove material's resistance to penetration by blood-borne pathogens and other virus-containing fluids, using a bacteriophage as a surrogate virus due to its small size and resistance. Gloves that meet this standard are vital in healthcare settings, laboratories, and any environment where there is a risk of exposure to viral infections. They are crucial for preventing the transmission of diseases, ensuring that workers are protected when handling potentially infectious materials, thus enhancing safety and health protocols in workplaces with biological hazards.
EN 374-2:2014 is a European standard that defines the performance requirements and test methods for chemical protective gloves against microorganisms. It specifies the minimum requirements for gloves to protect against microorganisms. The standard includes test methods for resistance to penetration by microorganisms and possible test results include pass/fail for each requirement.
Test results
Penetration Resistance TestedEN 374-2:2014 is an European Standard that specifies the requirements and test methods for evaluating the resistance of gloves to penetration by chemicals and/or microorganisms. In the test a glove is assessed for its capacity to resist penetration by micro-organisms or chemicals through pores, pinholes, or other imperfections. The test method involves inflating the glove with air or filling it with water and then examining it for leaks. This standard is important for ensuring that protective gloves do not allow harmful substances to reach the skin, thereby providing safety in chemical and biological environments.
EN 455-3:2015 is a European standard for disposable medical gloves. It sets out the definition, performance requirements and test methods for this type of gloves. The standard includes requirements for physical properties, dimensions, packaging, freedom from holes, freedom from powder, freedom from protein, freedom from endotoxins and freedom from pyrogens. Test results can include measurements of the gloves' physical properties, dimensions, packaging, freedom from holes, freedom from powder, freedom from protein, freedom from endotoxins and freedom from pyrogens. This version of the standard includes some changes and updates from the 2006 version.
EN 455-2:2015 is a European standard for disposable medical gloves. It sets out the definition, performance requirements and test methods for this type of gloves. The standard includes requirements for physical properties, dimensions, packaging, freedom from holes, freedom from powder, freedom from protein, freedom from endotoxins, and freedom from pyrogens. Test results can include measurements of the gloves' physical properties, dimensions, packaging, freedom from holes, freedom from powder, freedom from protein, freedom from endotoxins, and freedom from pyrogens. This version of the standard includes some changes and updates from the 2009 version.
Test results
Physical Properties TestedThe EN 455-2:2015 standard pertains to the physical properties of medical gloves, primarily focusing on ensuring they meet required levels of durability and performance under typical usage conditions. The designation that the physical properties were Tested under this standard implies that the gloves have undergone specific testing protocols to measure their tensile strength and elasticity and have been found compliant with predefined standards. The test method for physical properties under EN 455-2:2015 involves simulating conditions to mimic normal use and stresses that gloves would experience, such as stretching, which reveals both the elasticity and tensile strength of the material. Gloves undergoing these tests are stretched until they can stretch no further without breaking, and these results indicate whether the gloves are suitable for practical use in medical environments, offering users confidence in the durability and integrity of the gloves under operational conditions.
EN 455-1:2020 is a European standard for disposable medical gloves. It sets out the definition, performance requirements and test methods for this type of gloves. The standard includes requirements for freedom from holes, tensile strength, elongation, packaging, freedom from powder, freedom from protein, freedom from endotoxins, and freedom from pyrogens. Test results can include measurements of the gloves' freedom from holes, tensile strength, elongation, packaging, freedom from powder, freedom from protein, freedom from endotoxins and freedom from pyrogens. This version of the standard includes some changes and updates from the 2000 version.
Test results
Tightness AQL #,##EN 455-1:2020 sets the standards for medical gloves for single use, focusing on freedom from holes and ensuring glove integrity. The 'Tightness' test result, indicated by an Acceptable Quality Level (AQL) value, measures the quality level acceptable for the pinhole rate in glove batches. A lower AQL value, such as 1.5, typically used in medical settings, signifies a higher level of quality control where fewer gloves with defects are allowed. The testing for this standard involves randomly selecting gloves from a batch and filling them with water to check for leaks. Gloves that pass this test at a certain AQL value are deemed safe for use in medical and surgical procedures, where maintaining a sterile environment is crucial to prevent contamination and infection. This certification ensures that users can rely on the protective barrier of the gloves against pathogens and other contaminants.
EN 455-4:2009 is a European standard for disposable medical gloves. It sets out the definition, performance requirements and test methods for this type of gloves. The standard includes requirements for freedom from holes, dimensions, packaging, freedom from powder, freedom from protein and freedom from endotoxins. Test results can include measurements of the gloves' freedom from holes, dimensions, packaging, freedom from powder, freedom from protein and freedom from endotoxins.
ISO 13485:2016 is a standard that specifies requirements for a quality management system for the design and manufacture of medical devices. It includes requirements for how companies should design, implement, maintain and improve their quality management system to ensure that their medical devices are safe and effective. Test results can include information on how well the quality management system is functioning, how well it is being followed, and how effective it is in preventing defects. The standard also includes requirements for how the company should document and record their quality management system performance and continuously improve it.
Test results
Medical Management PassedThe ISO 13485:2016 standard is specifically tailored for medical device manufacturers and aims to ensure the quality and safety of medical devices throughout their production and lifecycle. A test result of Passed in the context of the ISO 13485:2016 standard signifies that the medical device manufacturing management system under assessment has successfully met all regulatory and safety requirements stipulated in the standard. This encompasses rigorous evaluations of the manufacturer's quality management system, including processes like risk management, regulatory compliance, and effective process control. The assessment involves auditing processes such as document review, facility inspection, and staff interviews, to verify the adequacy and effectiveness of the quality management system. Meeting the ISO 13485:2016 requirements assists manufacturers in achieving and maintaining regulatory compliance and ensures that their products consistently meet user needs and applicable regulatory standards, which is crucial for entry and continued presence in global markets.
EN ISO 9001:2015 is a standard that sets out the requirements for a quality management system (QMS). It is a set of guidelines that organizations can follow to ensure that they meet customer requirements and enhance customer satisfaction. The standard is based on the plan-do-check-act model and focuses on continuous improvement. It covers the design, development, production, installation, and servicing of products. Organizations can get certified to this standard, which means that they have been independently audited and found to meet the requirements of the standard. The certification process includes regular audits to ensure that the organization continues to meet the standard's requirements.
Test results
Service Reliability PassedEN 420:2003+A1:2009 is a European standard that sets out the general requirements for hand protection, including comfort, fit, and dexterity. Performance requirements include resistance to abrasion, cut, tear, puncture, and impact. Test results should show the gloves meet these requirements.
CE Marking is a label that shows a product meets certain safety and environmental standards set by the European Union. To get the CE Marking, a company must test and certify their product meets these standards. CE Marking is required for many products sold in the EU, including electronics, machinery, toys and medical devices. It helps ensure that products are safe for consumers and the environment, and allows for easy trade within the EU.
Food safe refers to the safety of food products that are used or consumed by people. In Europe, food safety is regulated by the European Union (EU) and the European Food Safety Authority (EFSA). These organizations set standards and requirements for food products to ensure they are safe to eat. To be considered "food safe" in Europe, a product must meet these standards and be free of harmful substances. This includes being free of harmful bacteria, pesticides, and other contaminants. Food products that do not meet these standards cannot be sold or used in the EU.
PPE stands for "personal protective equipment." PPE Category 3 refers to equipment that is complex and provide the highest level of protection such as powered respirators, SCBA, and full body suits. In Europe, PPE Category 3 must meet certain safety standards set by the European Union, which means that it must be designed and manufactured to protect the user without causing harm. Companies that make or sell PPE must prove that it meets these standards. They also must have a quality management system in place, have to be audited regularly by a notified body and have to have a technical documentation.
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Unigloves GM007 Advanced Heavy duty extended cuff purple nitrile gloves, 100 pcs
134,70 € / carton (VAT incl.)
107,33 €
A carton contains 10 packages (1 000 pcs)
10,73 € / 100 pcs
54 cartons / 54 000 pcs:
9,66 € / 100 pcs
In a package
100 pieces
In a carton
10 packages
1 000 pieces
On a pallet
54 cartons
54 000 piece
Unigloves
Delivery time: 10 business days
Orders from 1 200,00 €
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