Meditrade Suavel OP PRO Expert Coverall
Product description
DIN EN 13795 SP; 43g sterile
Measured in grams per square meter (g/m²), indicating fabric density and durability. Higher values offer more protection and insulation for demanding work environments.
Indicates the overall's hue, affecting visibility, stain-showing properties, heat reflection, and compliance with industry safety standards or team identification.
Defines how the overalls secure and fasten when worn, affecting ease of use, safety, and functionality in various work environments.
- Chemical Resistance
- Antimicrobial Protection
- Medical Protection
- Water Resistance
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Standards and labels
EN 556-1:2001 is a standard that explains how to sterilize medical equipment using steam. It tells you what temperature and pressure should be used during the sterilization process. The test results will show if the equipment is completely clean and free of germs, and if the sterilization process was done correctly.
EN ISO 11135-1:2007 is a standard that explains how to sterilize medical equipment using ethylene oxide gas. It tells you what temperature, humidity, and gas levels should be used during the sterilization process. The test results will show if the equipment is completely clean and free of germs, and if the sterilization process was done correctly.
EN 13795:2011 is a European standard that defines the performance requirements and test methods for surgical drapes, gowns, and clean air suits used in medical procedures. It sets guidelines for testing the barrier properties of the material, its resistance to penetration, its flame resistance, and its resistance to liquid penetration. The standard assigns each product a classification based on its performance in the test. Test results for products under this standard will show the product's classification, as well as its barrier properties, resistance to penetration, flame resistance properties and resistance to liquid penetration. This standard helps to ensure that the surgical drapes, gowns, and clean air suits used in medical procedures provide the appropriate level of protection and safety.
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.
Meditrade delivery terms
Free delivery for all Meditrade products
1 127,06 kr
Price per 1 package (30 pcs)
37,57 kr / piece
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