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Sterilization pouches (200 pcs/box) 57mm x 130 mm - SoftMed
- CE Medical Device
Self-adhesive paper-foil bags for steam sterilization
Resistant to tearing, resistant to moisture, dedicated to both small tools and larger sets of tools and clothing. They provide aseptic opening of the packaging. The indicators are placed in a way that prevents contamination of the contents of the bags.
They are available in sizes:
– 57x105mm
– 57x130mm
– 70x230mm
– 70x260mm
– 90x135mm
– 90x230mm
– 90x260mm
– 135x260mm
– 190x330mm
Properties of paper bag:
Self-adhesive bags do not require the use of a welding machine
Pre-complex to facilitate proper packaging closure
Equipped with thumb-cut at the top of the package to facilitate the package
External and internal indicator of the sterilization process
Printing outside the surface for direct contact with sterilized products
Foil with swab and tear-resistant
Made of special medical paper with a weight of 60 g/m2 and a 7-layer blue barrier film
Additional corner welds prevent the foil on the corners
A wide range of sizes allows for an economical selection of sterilization bags
How to use sterilization bags:
Tools and items are carefully placed in the bags, removing excess air from them before closing. The bags should be placed vertically, which facilitates the process of sterilization and drying. Two bags should be laid with a foil side and paper to paper.
Colored chemical indicators were printed on the bags indicating only sterilization. The confirmation of sterilisation should be indicated by an additional chemical or biological indicator.
After sterilization, do not allow for dampness, damage or accidental opening of bags.
Steering packages should be kept in accordance with the applicable state of law and the requirements of the sanitary authorities.
Method of storage:
The bags should be stored in a cool and dry place and protected from sunlight.
The shelf life is two years from the date of manufacture.
The marking:
Class I, in accordance with Regulation (EU) 2017/745 of the European Parliament and of the Council (EU) 2017/745 on Medical Devices (MDR) 2017/745 replacing Council Directive EC 93/42/EEC and Category 111 in accordance with the Regulation (EU) 2016/425.
Complies with standard: EN 868-5.