This is the category where claims discipline matters most, so we will start there rather than with the technology. An antibacterial textile is not a medical device and does not prevent infection or disease transmission. Anything that implies otherwise moves your product into a regulatory category with a different and much heavier burden of proof.
Healthcare textiles are laundered at high temperature and frequency, often industrially. A surface finish is designed to survive a consumer wash cycle, not an industrial one repeated hundreds of times. PLATARI is a pre-treatment: nano platinum, silver and zinc are compounded into masterbatch and spun into the fibre, so function sits inside the yarn cross-section rather than on its surface.
| Antibacterial | SGS >99.9% against common strains |
|---|---|
| Supply forms | Masterbatch · yarn · finished fabric |
| Skin contact | Function is inside the fibre rather than a surface chemistry against the skin |
Wash durability under your laundering protocol, skin-contact testing appropriate to your market, and any biocompatibility work your product class requires. We supply material and the manufacturer's test documentation; the qualification is yours.
No, and we will not let that be implied. Protective performance comes from filtration and fit. An antibacterial inner layer addresses odour and microbial growth in the fabric itself, which is a comfort and hygiene benefit, not a protective one.
In most markets you can describe the treatment as protecting the textile. Claiming it protects the wearer from infection is a different and far more restricted claim. Confirm final wording with your compliance team.
In-fibre function does not wash off the way a surface finish does, but retained performance under your specific industrial protocol must be measured on your fabric.
No. It is a functional textile material. If your finished product is a medical device, that classification and its evidence requirements are yours to manage.
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