Abena Protective Sheet Standard 80x170cm
Product description
The product description has not been specified
Indicates the measured length in meters of the hygiene product, helping determine coverage area and usage duration for cleaning and sanitation tasks.
Identifies the primary substance composition affecting product performance, durability, safety, and environmental impact in hygiene applications.
Measurement across the underpad that determines coverage area and fit for beds, chairs, or examination tables. Proper width ensures optimal protection.
The visual appearance that may indicate purpose in color-coded cleaning systems, match facility aesthetics, or help identify product types in various environments.
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Standards and labels
Dermatologically Tested refers to products that have been tested and proven to be safe for use on the skin. The European Union has regulations for cosmetics products, which includes dermatological testing, to ensure that products are safe for use. To be labeled as dermatologically tested, the product must be tested by a qualified professional, such as a dermatologist, and must not cause any irritation or allergic reactions. The testing must be carried out on a representative sample of human volunteers and the results must be evaluated by a qualified professional before the product can be considered as dermatologically tested and can bear the label. The EU Cosmetics Regulation, lays out the specific requirements for safety assessments and labeling of cosmetics products.
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.
FSC Mix is a label that indicates that a product contains a mix of wood from both responsibly managed forests (FSC certified) and other sources. In Europe, to use the FSC Mix label, a company must ensure that the wood used in the product is from legal and responsibly managed sources. Additionally, the company must have a system in place to track the wood used in the product and be able to prove that it comes from a mix of FSC certified and other sources.
Standards have not been specified
Abena Ab delivery terms
Free delivery when you order more than 1 650,00 kr from Abena Ab
Supplier shipping fee 55,20 kr
Brand minimum 0,00 kr
Price available on request
Shipping fee is 55,20 kr for orders under 1 650,00 kr
A carton contains 5 packages (125 pieces)
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Abena Ab
Delivery time: 3 business days
Supplier shipping fee 55,20 €
Free shipping on orders over 1 650,00 €



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