EN 868-5 Packaging for Sterilized Medical Devices, Part 5: Sealed Bags and Reels of Porous Materials and Plastic Film Making

Packaging Tests

EN 868-5 Packaging for Sterilized Medical Devices, Part 5: Sealed Bags and Reels of Porous Materials and Plastic Film Making

EUROLAB, with its state-of-the-art accredited laboratories and expert team, provides precise and fast testing services within the scope of EN 868-5 testing. This standard specifies test methods and values ​​for sealable bags and reels made of porous materials and plastic film conforming to EN 868 part 2, 3, 6, 7, 9 or 10.

EN 868-5 Packaging for Sterilized Medical Devices, Part 5: Sealed Bags and Reels of Porous Materials and Plastic Film Making

These sealable bags and reels are used sterile. Finally, they are barrier systems or packaging systems that are intended to maintain the sterility of sterilized medical devices until the point of use.

Except for the general requirements specified in EN ISO 11607-1 and EN ISO 11607-2, this part of EN 868 specifies materials, test methods and values ​​specific to products covered by this standard. The materials specified in this part of EN 868 are for single use only.

EUROLAB assists manufacturers with EN 868-5 test compliance. Our test experts, with their professional working mission and principles, provide you, our manufacturers and suppliers, the best service and controlled testing process in our laboratories. Thanks to these services, businesses receive more effective, high-performance and quality testing services and provide safe, fast and uninterrupted service to their customers.

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