
Meditrade Reference™ Latex Examination Glove, Powdered
Meditrade Reference™ Latex Examination Glove, Powdered
4.8 / 5


Features You'll Love

Finger Thickness · 0.11 mm
Measures the material thickness at the fingertips, affecting tactile sensitivity...
Meditrade Reference™ Latex Examination Glove, Powdered
4.8 / 5
430,93 kr
516,92 krPrice per 10 packages (1 000 pcs)
43,09 kr / 100 pcs
Free delivery
Features You'll Love

Finger Thickness · 0.11 mm
Measures the material thickness at the fingertips, affecting tactile sensitivity...
Product description
The product description has not been specified
Indicates whether gloves contain powder on the interior surface to aid donning, affecting ease of use and contamination control requirements.
Measures the thickness of the glove's wrist/forearm extension, affecting durability, tear resistance, and protection level during use.
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.
Measures how far the glove extends up the wrist and forearm, determining the level of coverage and protection provided during use.
Describes the surface texture of the fingertip area, affecting grip strength and tactile sensitivity during use.
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.
Complete finger coverage ensures full protection and hygiene for your hands, maintaining dexterity for all tasks.
Measures the material thickness at the fingertips, affecting tactile sensitivity, dexterity, and protection level during use.
Indicates the maximum percentage of defective gloves acceptable in quality testing, with lower numbers representing higher quality standards.
Measures the material thickness at the palm area, affecting protection level and tactile sensitivity during use.
- Clean Room
- Food Service
- Slip Resistant
- Medical Protection
- Hand Protection
Medical gloves with the EN 455-3:1999 rating are tested for biological safety, specifically evaluating levels of proteins and leachable substances. This ensures the gloves minimize potential allergic reactions and harmful effects for both the wearer and patient, providing peace of mind.
Test results
This product has been tested for biological safety to ensure it is safe for skin contact. It minimizes the risk of adverse reactions from chemicals, latex proteins, and other residues used during manufacturing.
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.
Test results
This product is tested for physical strength and durability to ensure reliable performance. It meets specific requirements for size, stretch, and force-at-break, providing adequate protection against cross-contamination for both the user and patient.
Medical gloves for single use with the EN 455-1:2020+A1:2022 rating are tested for freedom from holes and leakage. This ensures the gloves provide a reliable barrier, minimizing the risk of contamination for your safety and protection.
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.
Medical devices with the ISO 13485:2016 rating are tested for a quality management system that ensures consistent safety, quality, and regulatory compliance throughout their lifecycle. This provides assurance that the product is reliably produced to high international standards for patient use.
Test results
This product was made under a quality management system that ensures consistent design, production, and distribution. This focuses on the safety, performance, and regulatory compliance of medical devices throughout their entire lifecycle, from design to disposal.
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.
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