Over 40,000 satisfied customersHygostar Type II PP Face Masks
Franz Mensch Nordics
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Product description
The product description has not been specified
Indicates the level and type of filtration provided, determining what contaminants the respirator protects against and the percentage of particles filtered.
Determines the physical form of the mask, affecting comfort, breathing space, storage convenience, and how well it seals against your face.
The method used to secure the respirator to your face, affecting comfort, fit, and ease of putting on and removing the mask.
Determines the coverage area and design of the respirator, such as full face or half face, affecting protection level and compatibility with other safety equipment.
Measures the percentage of bacteria-sized particles filtered out, indicating the respirator's effectiveness at blocking biological contaminants.
- Respiratory Protection
- Medical Protection
- Antimicrobial Protection
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Standards and labels
Medical face masks with the EN 14683:2019 rating are tested for bacterial filtration efficiency, breathability, splash resistance, and microbial cleanliness. This means the mask has been assessed to help limit the spread of infective agents while allowing you to breathe comfortably.
Test results
Bacterial Filtration Type IIThis medical face mask filters at least 98% of bacteria. It is intended for use in medical settings to prevent the transmission of infectious agents from staff to patients and is also suitable for public use.
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.
Franz Mensch Nordics delivery terms
Free delivery when you order more than 150,00 € from Franz Mensch Nordics
Supplier shipping fee 6,33 €
Brand minimum 0,00 €
29,07 €
Price per 20 packages (1 000 pcs)
0,029 € / piece
Shipping fee is 6,33 € for orders under 150,00 €
A carton contains 20 packages (1 000 pieces)
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