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Granberg 630, Nitrile Gloves
-16%

Granberg Nitrile Gloves

7,07 € / 100 pcs

(19)

Granberg Nitrile Gloves

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(19)

Prices excl. VAT
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141,45 €

168,69 

Price per 10 packages (2 000 pcs)


7,07  / 100 pcs

Estimated delivery: Thu Oct 23
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Features You'll Love

Surface · Smooth feature highlight

Surface · Smooth

The texture of the glove exterior, affecting grip strength and handling capabili...

Cuff Style · Rolled feature highlight

Cuff Style · Rolled

The design of the wrist opening, affecting ease of putting gloves on, comfort, a...

Product description

Granberg Magic Touch disposable gloves 200 pieces in a pack (XL size 180 pieces).

Soft and durable thin protective glove. Thinner than usual nitrile gloves are suitable for use in healthcare, food processing and other personal protection applications.

  • Describes the surface texture of the fingertip area, affecting grip strength and tactile sensitivity during use.

  • Provides comfort and peace of mind, free from natural rubber latex to protect sensitive skin.

    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.

  • 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.

  • 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.

  • Total mass of the glove package, useful for shipping calculations, storage planning, and comparing product quantities across different brands.

  • The design of the wrist opening, affecting ease of putting gloves on, comfort, and how securely they stay in place during use.

  • Measures the material thickness at the palm area, affecting protection level and tactile sensitivity during use.

  • Hand Protection
  • Chemical Resistance
  • Food Service
  • Medical Protection
  • Antimicrobial Protection
  • Medical gloves with the EN 455-1:2000 rating are tested for freedom from holes, primarily using a water leak test. This ensures the gloves provide a reliable, intact barrier, protecting both the user and patient from cross-contamination during medical procedures.

  • Single-use medical gloves with the EN 455-2:2015 rating are tested for physical properties like dimensions and strength. This ensures gloves fit correctly and are strong enough to provide reliable protection without tearing during use.

  • Medical gloves with the EN 455-3:2015 rating are tested for biological safety, including protein, endotoxin, chemical, and powder content. This ensures the gloves are safe for use, reducing risks of allergic reactions and irritation for consumers.

  • Single-use medical gloves with the EN 455-4:2009 rating are tested for their shelf life, ensuring they maintain properties like strength and barrier integrity over time. This means the gloves will remain effective and safe, providing reliable protection against infections until their expiration date when stored correctly.

  • Protective gloves with the EN ISO 374-1:2016/A1:2018 rating are tested for resistance against dangerous chemical penetration, permeation, and degradation. This means the gloves are proven to protect your hands from hazardous substances and indicate how long they can withstand contact with specific chemicals.

    Test results

    These gloves provide basic, short-term protection against at least one specific chemical. They are suitable for tasks involving minimal chemical splash risk, offering a barrier for at least 10 minutes against permeation.

  • Protective gloves with the EN 420:2003+A1:2009 rating are tested for general design, safe materials (innocuousness), water penetration, comfort, and dexterity. This ensures the gloves are safe, fit correctly, and allow you to perform tasks effectively without discomfort.

  • Protective gloves with the EN 374-4:2013 rating are tested for their resistance to degradation by chemicals. This measures changes in the glove material, like swelling or hardening, ensuring the glove maintains its protective qualities when exposed to hazardous substances.

  • Gloves with the EN 374-5:2016 rating are tested for resistance to penetration by bacteria and fungi, and potentially viruses. This means the gloves provide a protective barrier against microorganisms, helping to keep your hands safe from harmful biological agents.

    Test results

    This glove is tested to protect you from bacteria, fungi, and viruses. It provides a reliable barrier, having passed specific tests to ensure no leakage when exposed to these micro-organisms, making it suitable for handling contaminated materials.

  • 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 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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