Hydropump
- Risk class
- Class I
- CND nomenclatures code
- V9099
- Trade name
- XERSIZER PRO NINE X
- Implantable
- No
- Reusable
- No
- Measuring function
- No
- Primary DI
- 05060140208631
- Basic UDI
- 506014020DXP9J
- Version date
- October 10, 2022
- Manufacturer last update
- October 11, 2021
- Active status
- No
- Manufacturer name
- DX Products Limited
- Country
- United Kingdom (ex Northern Ireland)
- Country type
- NON_EU
- Address
- Unit 1 Horbury Junction Industrial Estate, Caldervale road Wakefield
- mark@bathmatedirect.com
- SRN
- IE-AR-000001724
- Country
- Ireland
- Address
- 12a, Office 2 Lower Main Street Co. Dublin
- info@ecrep-caresurgical.com
- Telephone
- +35312460099
- Competent authority
- Health Products Regulatory Authority, Medical Devices Department
- Applicable legislation
- MDR (REGULATION (EU) 2017/745 on medical devices)
- Placed on the market
- United Kingdom (Northern Ireland only)
- Human tissues
- No
- Animal tissues
- No
VARIOUS DEVICES NOT INCLUDED IN OTHER CLASSES - OTHER
Access comprehensive regulatory information for Hydropump in the European Union medical device market through Pure Global AI's free database. This Class I device is registered with EU EUDAMED under Primary DI 05060140208631 and manufactured by DX Products Limited in United Kingdom (ex Northern Ireland).
This page provides complete registration details including trade name (XERSIZER PRO NINE X), manufacturer information, authorized representative details, competent authority (Health Products Regulatory Authority, Medical Devices Department), and regulatory compliance data from the official EU EUDAMED medical device database. Pure Global AI offers free access to the European Union's complete medical device registry, helping global MedTech companies navigate EU MDR regulations efficiently.