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Ostomy Pouch Manufacturer — One-Piece, Two-Piece and OEM Supply

Hydrocolloid barriers from 0.8 to 1.2 mm, EVOH odour film, cut-to-fit range 15–60 mm, optional validated EO sterilisation — built to your market's registration route.

Why us

A factory, not a repacker

Hydrocolloid barrierEVOH odour filmCut-to-fitEO sterilisation

An ostomy pouch is the hardest thing we make. It has to hold on skin that is wet, moving and often uneven, and it has to do it without warning. Failure rarely happens in the bag; it happens at the barrier edge, at three in the morning, on a person who then stops trusting the product.

So we spend the engineering where failure happens: barrier adhesion and erosion under output, cut-to-fit accuracy, and odour film gauge. We publish the parameters we can prove, and we will not write a claim into your artwork that the certificate pack does not support.

At a glance

The seven answers buyers ask for first

Barrier Medical hydrocolloid, 0.8–1.2 mm
Cut range 15–60 mm, printed sizing rings
Film EVOH co-extrusion, 80–120 µm
Filter Charcoal odour filter, optional
Sterilisation EO, validated cycle, optional
MOQ From 100 pouches per construction
Documents Spec, CoA per lot, sterilisation records
Specification

What you can specify

Ostomy constructions are market-specific. The rows below are where yours will differ.

TypeOne-piece closed, one-piece drainable, two-piece, urostomy
BarrierHydrocolloid 0.8–1.2 mm, flat or convex
Cut range15–60 mm with printed rings; pre-cut sizes also available
Pouch filmEVOH co-extrusion 80–120 µm, opaque or translucent
ClosureIntegrated clip, drainable outlet, urostomy tap
FilterCharcoal filter with gas-release membrane
SterilisationEO validated cycle; non-sterile bulk also supplied
PackingPoly bag plus printed carton; shelf-ready carton on request
LabellingLanguage set and symbols per destination market
Process

From enquiry to delivery

Medical projects take longer at the front and shorter at the back. We plan it that way.

1

Brief & market

Pouch type, stoma range, market and the registration route you are on.

2

Construction

Barrier, film, filter and closure proposed against your sample or spec.

3

Sample

Pilot samples for wear and fit evaluation, with parameters recorded.

4

Validation

Process parameters fixed, sterilisation cycle validated where required.

5

Mass run

Scheduled production with lot traceability, CoA per lot and export packing.

Quality control

What we check before it ships

For a medical device the record matters as much as the test. Ask for both.

  • Barrier thickness and adhesive coat weight
  • Cut-ring print accuracy and die dimension
  • Pouch seal strength, all seams
  • Leak test on finished pouch
  • Filter function and odour check
  • Sterilisation record and lot linkage
Start here

Send your current product, or just the idea

A physical sample is ideal, a drawing works, and a written brief is enough to start. We quote against your market and claim limits.

WhatsApp +86 185 5818 2356 Mon–Fri 09:00–18:00 (GMT+8) shine@horpulse.com Quotes, datasheets and samples all go through this address

Tell us what you’re building

Five fields. We reply within one business day with a workable route and pricing path.

By sending, you agree to be contacted by email or WhatsApp about this enquiry. Your details are used for this conversation only.

Buyer questions

Buyer questions

Yes. Our minimum starts from 100 pouches per construction, which is meant for clinical evaluation and fit trials rather than resale. Commercial volumes are quoted separately, because barrier, film and closure choices move the price more than quantity does.
Yes, that is the normal route. Artwork, language set, symbols and carton layout are yours; we confirm the label content against the claims your registration supports before printing.
We supply both sterile and non-sterile. Sterile pouches go through a validated EO cycle with records kept per lot; non-sterile bulk is supplied for markets or customers that sterilise locally.
Specification, material statements, CoA per lot, sterilisation records and process validation documentation are available under NDA. Certificate status per market is published on our Quality & Regulatory page — check it before writing claims.
About a week after sample approval for standard constructions, confirmed against the order schedule. New tooling, custom film or a validated sterilisation cycle adds time at the front, not at the end.
Ostomy pouch manufacturer Reply in one business day, with MOQ and lead time
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