JSP 500ml Eyewash Solution
Product description
A 500ml container of emergency eyewash Sterile solution of Sodium 0.9 w/v (Normal Saline) Can be used to refill the wall-mounted stations
Packaging format that affects product sterility, ease of access, and application method. Important for ensuring proper storage and efficient use during first aid situations.
Indicates the volume of eye wash solution available for emergency treatments, affecting usage duration and compliance with workplace safety standards.
Identifies the substance composition of first aid products, affecting skin compatibility, absorption capacity, breathability, and durability during wound treatment.
Indicates key properties like sterility, reusability, or special features that determine suitability for specific wound care scenarios and workplace requirements.
- Medical Protection
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Standards and labels
Sterile refers to the absence of living microorganisms, including bacteria, viruses, fungi and spores. Sterility is achieved through various methods such as cleaning, filtration, radiation, and chemical treatments. Sterility is a requirement in many medical and laboratory settings, as well as in the production of certain food and drink products. The requirements for a sterile product or environment will depend on the specific application, but generally it should be free from any living microorganisms, it should be easy to maintain and keep clean, it should be safe for people to use, it should be able to maintain its sterility over time. Sterility is important in many medical and laboratory settings, as well as in the production of certain food and drink products to ensure that they are safe for consumption.
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.
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.
Standards have not been specified
JSP Safety delivery terms
Free delivery when you order more than 1 650,00 kr from JSP Safety
Supplier shipping fee 69,00 kr
Brand minimum 5 500,00 kr
904,01 kr
Price per 10 pcs
90,40 kr / piece
See your personal discount by adjusting the quantity
Need larger quantities?
A carton contains 10 packages (100 pieces)
Example amount
Price & savings
88,21 kr / piece
85,84 kr / piece
84,40 kr / piece
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JSP Safety
Delivery time: 4 business days
Orders from 5 500,00 €
Supplier shipping fee 69,00 €
Free shipping on orders over 1 650,00 €



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