Nitras Medical VINYL PF vinyl disposable gloves, transparent
Product description
Professional-grade vinyl disposable gloves designed for medical examination and food handling applications. These powder-free gloves are manufactured according to EN 455 standards with an AQL 1.5 rating for consistent quality assurance. The ambidextrous design and rolled edge provide versatile use and enhanced comfort during extended wear.
Product Features:
- Powder-free construction
- Rolled edge for improved comfort
- Ambidextrous design
- Non-sterile
- Uniform 0.06mm thickness
Technical Details:
- Material: 100% Vinyl
- Elongation at break: minimum 300%
- Tensile strength: minimum 11 MPa
- AQL 1.5 quality rating
Standards:
- EN 455 medical gloves certification
- Food contact approved
Recommended Applications:
- Medical examinations
- Food handling and processing
Measures the material thickness at the wrist area, affecting barrier protection, durability, and how well the glove stays in place during use.
Indicates the statistical quality inspection standard measuring defect rates. Lower AQL values (e.g., 0.65) signify fewer defects and higher protection reliability.
Measurement of material thickness in the palm area, affecting protection level, durability, and dexterity. Critical for matching gloves to specific tasks.
Measures from fingertip to cuff end, determining wrist/forearm coverage. Longer gloves provide enhanced protection against splashes and contaminants.
Measures the material thickness in the finger areas, balancing protection against punctures and chemicals with tactile sensitivity for precision tasks.
Describes whether fingertips have a smooth or textured surface, affecting grip strength, tactile sensitivity, and handling precision for various applications.
Indicates the composition of the gloves, affecting properties like elasticity, chemical resistance, allergen potential, and suitability for specific tasks.
Indicates the glove's pigmentation, which can aid in color-coding tasks, enhancing visibility, or meeting specific industry requirements for contamination control.
Refers to whether gloves have a smooth or textured finish, affecting grip strength, dexterity, and handling ability in wet or dry conditions.
Indicates whether gloves contain donning powder. Powder-free options reduce allergen risks and contamination, while powdered versions offer easier application.
Defines how the wrist portion of the glove is finished, affecting ease of donning, security during use, and resistance to tearing when putting on.
Designed for use on either hand, these gloves offer convenience and efficiency. Their symmetrical design simplifies donning and reduces waste.
Ideal for handling items like produce or baked goods, these gloves resist degradation from non-fatty foods, ensuring food safety and hygiene.
- Hand Protection
- Food Service
- Medical Protection
- Antimicrobial Protection
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Standards and labels
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.
MD stands for "Medical Device." It refers to any instruments, apparatus, machines, implants, or other similar or related articles that are intended to be used for human beings for the purpose of diagnosis, prevention, monitoring, treatment or alleviation of disease, injury or disability. In Europe, a MD Label is a special label that must be on all Medical Devices that are sold or used in the European Union (EU). The label must include information about the product, such as the name of the manufacturer, the intended use of the product and CE mark. To be able to sell or use a Medical Device in the EU, the device must meet certain standards and requirements set by the European Union and notified body.
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.
Nitras delivery terms
Free delivery when you order more than 150,00 € from Nitras
Supplier shipping fee 4,74 €
Brand minimum 90,00 €
27,20 €
Price per 10 packages (1 000 pcs)
2,72 € / 100 pcs
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Nitras
Delivery time: 4 business days
Orders from 90,00 €
Supplier shipping fee 4,74 €
Free shipping on orders over 150,00 €



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