The pressure sensitive range includes a named medical category. Medical and care disposables — the dressings, tapes, drapes, protective items and hygiene-adjacent products that converters produce for healthcare channels — use pressure sensitive adhesive as a functional layer: fixing a dressing component, laminating a film to a nonwoven, or providing the skin- or surface-contact tack the product is designed around. The manufacturer's documented medical listings sit inside that converting reality, and they are specified the way converters actually buy: per product construction, per line, per test regime.
Medical buyers should read this page against their own regulatory file. The manufacturer documents a medical adhesive category and medical among its application industries; medical-device certifications, biocompatibility results and regulatory clearances for these grades are not published here. State exactly the documents your regulatory file requires in the enquiry — certificates are available upon request, and the documents that can be provided for your product are confirmed in the reply. Any grade for a medical product must be qualified by the converter's own testing for their product and market.
How Medical Grades Are Specified
A medical adhesive enquiry should name the product construction (which layers the adhesive joins, or whether it is the contact layer), the converting method and line speed, the sterilisation or packaging route if any, and the documentation the buyer's regulatory file requires. Those four points decide whether a documented grade can be quoted directly or whether the customisation route — performance brief, formulation, sample, performance test — is the honest path. Skin-contact performance, residue and ageing are product-level qualifications; they are established by the converter's testing on the finished construction, not asserted by an adhesive catalogue.
Medical channels punish vague claims, so the enquiry route is the working route: name the documents your regulatory file requires, and the manufacturer confirms in the reply which of them can be provided for the grade quoted, alongside samples supplied against your brief.
How to Specify This Adhesive
A useful enquiry names five things: the substrate or material being bonded, the application method and equipment, the coat weight in grams per square metre where it is known, the temperature the bond must withstand in service, and the test standard your customer applies. Those five points are the same starting points the manufacturer's own customisation process uses when it opens a new formulation brief, and they let the laboratory match an existing grade before anyone talks about developing a new one.
If you are replacing an adhesive already in production, send its current grade name or a sample description — viscosity behaviour, colour and the failure you are trying to fix (edge lifting, ooze, stringing, cold failure) narrow the choice faster than a catalogue number. Samples are part of the documented route: free samples are listed on many product pages, and the freight arrangement for your sample is confirmed in the reply.
Supply, Packing and Samples
The documented minimum order on product listings is 1,000 kg, consistent with the 1-tonne minimum stated in the manufacturer's published frequently asked questions, and the documented production cycle is 7–15 days. Packing follows the listing for the grade — film-wrapped blocks are the standard form, with carton packing stated per product — and can be confirmed against your handling requirements in the quotation. Nothing on this page promises a grade's availability before the quotation confirms it for your specification.
What medical products use these grades?
The medical category serves medical and care disposable converting — dressings, tapes and related constructions. Your product construction decides the grade; describe it in the enquiry.
Are medical certifications published on this page?
The manufacturer's general systems are named as ISO 9001, REACH and SGS tested. Product-specific documentation is requested per file — certificates are available upon request, and what can be provided for your product is confirmed in the reply.
Can a grade be developed for a medical construction?
The documented customisation process exists for exactly this: brief, formulation, sample, performance test. Regulatory qualification of the finished product remains the converter's responsibility.
Send the application, substrate, application method and the quantity you need — the grade, sample route and price are confirmed per product in the written quotation.
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