Over 40,000 satisfied customersAldena Blue Nitrile Gloves Powder Free
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Product description
The product description has not been specified
Measures how far the glove extends up the wrist and forearm, determining the level of coverage and protection provided during use.
Indicates the maximum percentage of defective gloves acceptable in quality testing, with lower numbers representing higher quality standards.
Indicates how long gloves maintain their protective properties and quality when stored properly, typically measured in years from manufacture date.
Describes the surface texture of the fingertip area, affecting grip strength and tactile sensitivity during use.
Easily wear on either hand, ensuring quick protection and less waste.
Provides comfort and peace of mind, free from natural rubber latex to protect sensitive skin.
Indicates whether gloves contain powder on the interior surface to aid donning, affecting ease of use and contamination control requirements.
The texture of the glove exterior, affecting grip strength and handling capability for different tasks and working conditions.
The visual appearance of the glove material, ranging from basic colors to specialized options for different professional and aesthetic preferences.
The base substance used to manufacture the glove, affecting chemical resistance, durability, flexibility, and compatibility with specific applications.
- Hand 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.
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 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.
Aldena delivery terms
Free delivery for all Aldena products
27,52 €
Price per 10 packages (1 000 pcs)
2,75 € / 100 pcs
Free delivery
A carton contains 10 packages (1 000 pieces)
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