Over 40,000 satisfied customersUnigloves Unicare Clear vinyl gloves
Unigloves
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Product description
• AQL 1.5 and EN455 parts 1-4
• Free from latex and accelerators
• Free from powder
• Tested to EN1186
• Ambidextrous
• Manufactured using high-quality vinyl
• Beaded cuff
• Medium-weight construction
• Touchscreen compatible
The texture of the glove exterior, affecting grip strength and handling capability for different tasks and working conditions.
Total mass of the glove package, useful for shipping calculations, storage planning, and comparing product quantities across different brands.
Indicates how long gloves maintain their protective properties and quality when stored properly, typically measured in years from manufacture date.
Measures the material thickness at the palm area, affecting protection level and tactile sensitivity during use.
Measures how far the glove extends up the wrist and forearm, determining the level of coverage and protection provided during use.
The base substance used to manufacture the glove, affecting chemical resistance, durability, flexibility, and compatibility with specific applications.
Describes the surface texture of the fingertip area, affecting grip strength and tactile sensitivity during use.
The visual appearance of the glove material, ranging from basic colors to specialized options for different professional and aesthetic preferences.
Gentle on sensitive skin, these gloves are free from common chemical accelerators, reducing irritation for comfortable, worry-free wear.
Effortlessly use touch screens without removing your gloves, ensuring continuous protection and hygiene.
Provides comfort and peace of mind, free from natural rubber latex to protect sensitive skin.
Ensures safe, hygienic handling of non-fatty foods, protecting both your hands and the food.
Your go-to gloves for diverse tasks, offering reliable protection and convenience across many applications.
Easily wear on either hand, ensuring quick protection and less waste.
Indicates whether gloves contain powder on the interior surface to aid donning, affecting ease of use and contamination control requirements.
Measures the material thickness at the fingertips, affecting tactile sensitivity, dexterity, and protection level during use.
Measures the thickness of the glove's wrist/forearm extension, affecting durability, tear resistance, and protection level during use.
Indicates the maximum percentage of defective gloves acceptable in quality testing, with lower numbers representing higher quality standards.
- Clean Room
- Food Service
- Medical Protection
- Antimicrobial Protection
- Hand Protection
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Standards and labels
EN ISO 21420:2020 is a European standard that sets out the general requirements for hand protection, including comfort, fit, and dexterity.
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.
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 455-2:2009 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 physical properties, dimensions, packaging, freedom from holes, freedom from powder and freedom from protein. Test results can include measurements of the gloves' physical properties, dimensions, packaging, freedom from holes, freedom from powder and freedom from protein. This version of the standard includes some changes and updates from the 2000 version.
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.
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.
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 1 refers to equipment that is simple and easy to use, and has a lower level of risk. Examples of PPE Category 1 include gloves, goggles, and simple respirators. In Europe, PPE Category 1 must meet certain safety standards set by the European Union. This 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.
Unigloves delivery terms
Free delivery when you order more than 150,00 € from Unigloves
Supplier shipping fee 6,33 €
Brand minimum 1 200,00 €
24,91 €
Price per 10 packages (1 000 pcs)
2,49 € / 100 pcs
Shipping fee is 6,33 € for orders under 150,00 €
A carton contains 10 packages (1 000 pieces)
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