Sourcing urinary catheters from China
Urinary catheters from China carry 0% UK duty under 9018 39 00 00, with no trade remedy in the supplied tariff record. Before sale in Great Britain, devices need MHRA registration and the Chinese manufacturer needs a UK Responsible Person. Match the documentation to the exact catheter. Cambridge China Bridge sources urinary catheters.

Urinary catheter duty and classification
Heading 9018 covers medical, surgical, dental and veterinary instruments and appliances. Urinary catheters fall within the catheters, cannulae and similar goods line, 9018 39 00 00. The table shows catheter variants sharing this commodity line, rather than separate tariff subdivisions.
Read from the UK Trade Tariff on 8 October 2026, the catheter line carries 0% duty for goods from China. The supplied record lists no anti-dumping or countervailing duty, suspension or attached import control for this line. This does not remove medical device obligations.
Confirm the commodity code against the catheter description and contents of any supplied kit. For other goods within the heading, see disposable syringes.
| Goods | Commodity code | Duty | Anti-dumping or countervailing duty on China |
|---|---|---|---|
| Silicone balloon urinary catheters | 9018 39 00 00 | 0% | None |
Specify the catheter and its intended use
Separate intermittent catheters from indwelling balloon catheters. Specify material, latex content, coating, shaft diameter, usable length, tip shape, drainage eyes and connector. For balloon products, agree the labelled inflation volume, inflation medium and balloon testing. For coated products, define activation instructions and the supplied lubricant or fluid. For adult incontinence pants, see our incontinence pants sourcing guide.
Ask for the manufacturer's classification rationale, declaration of conformity and applicable conformity assessment certificates for the exact model. Confirm the accepted CE or UKCA route for Great Britain before ordering. Obtain sterilisation validation, sterile barrier packaging evidence and shelf-life support matching the finished catheter and packaging.
A Chinese manufacturer must appoint a UK Responsible Person, and devices must be registered with the MHRA before placement on the Great Britain market. The importer must notify the manufacturer or UK Responsible Person of its intention to import; they submit the importer details to the MHRA. These paragraphs concern Great Britain. For UK-to-China trade, see our guide to exporting medical devices to China.
Worked duty example
Illustrative example, not a quote: Illustrative small-business batch of assorted urinary catheters under 9018 39 00 00, invoiced at £10,000 free on board, with £900 of freight and insurance to the UK. The customs value is £10,900. Duty at 0% is £0. Import VAT at 20% is charged on the customs value plus duty, £10,900, so it is £2,180. With no duty, the only import tax is the VAT, which a VAT-registered importer can usually reclaim. The import duty and VAT guide explains each step.
Inspection checklist
Identity: match material, latex declaration, dimensions, tip, coating and connector to the approved sample and purchase specification.
Function: use designated test samples to check drainage, balloon inflation and deflation, valve leakage and coating activation against agreed methods. Keep opened samples separate from saleable sterile stock.
Packaging: examine pouch seals, punctures, moisture and carton damage. Match English instructions, product references, lot numbers and expiry dates to the approved artwork and batch documents.
Records: match sterilisation release records and packaging evidence to the delivered lots. Visual inspection cannot establish sterility. Plan checks through quality inspection.
Working out your own order? Send us the product on WhatsApp and we reply the same working day: WhatsApp us
What goes wrong
Look for rough drainage eyes, kinked tubing, leaking inflation valves, balloons that fail to deflate as specified and uneven coating activation. Material substitutions or changed packaging can also leave the delivered product outside the specification supported by the supplier's documents.
Quarantine affected lots when seals are damaged, labels conflict or batch evidence is missing. Ask the manufacturer to investigate before release. MHRA registration is not accreditation, certification, approval or endorsement, so a registration entry alone does not establish that the catheter meets its requirements.
Cambridge China Bridge sources these products for UK businesses, checking the factory and the documents before shipment. See factory verification. For components and parts, see sourcing for manufacturers.
Frequently asked questions
What is the UK import duty on urinary catheters from China?
The supplied tariff record shows 0% under 9018 39 00 00, with no anti-dumping or countervailing duty, suspension or attached import control on that line.
Does a Chinese catheter manufacturer need a UK Responsible Person?
Yes, for the Great Britain market. A manufacturer outside the UK must appoint a UK Responsible Person, and the devices must be registered with the MHRA before placement on that market.
Does MHRA registration mean the catheter is approved?
No. MHRA registration does not represent accreditation, certification, approval or endorsement. Check the conformity documents and evidence for the exact product.
What should I check when sterile catheters arrive?
Check pouch seals, damage, product references, lot numbers, expiry dates and English instructions. Match the lots to sterilisation release records; appearance alone cannot establish sterility.