Venous Blood Collection Kit, Professional Use
- Risk class
- Class A
- CND nomenclatures code
- W0501010199
- Trade name
- Venous Blood Collection Kit, Professional Use
- Implantable
- No
- Reusable
- No
- Measuring function
- No
- Primary DI
- 05056751600926
- Basic UDI
- 50567516MDTF0053P5
- Version date
- December 23, 2024
- Manufacturer last update
- January 15, 2025
- Active status
- No
- Manufacturer name
- REAL Digital International Ltd
- Country
- United Kingdom (ex Northern Ireland)
- Country type
- NON_EU
- Address
- 2 Queensway CR0 4BD Croydon
- Bayode-Adisa@real-digital.co.uk
- SRN
- NL-AR-000037688
- Country
- Netherlands
- Address
- 2b Lange Viestraat Utrecht
- eurep@casusconsulting.com
- Competent authority
- Ministerie van Volksgezondheid, Welzijn en Sport
- Applicable legislation
- IVDR (REGULATION (EU) 2017/746 on in vitro diagnostic medical devices)
- Placed on the market
- United Kingdom (Northern Ireland only)
- Market available
- Ireland:None~None, United Kingdom (Northern Ireland only):None~None
- Human tissues
- No
- Animal tissues
- No
VENOUS OR ARTERIOUS BLOOD COLLECTION DEVICES - OTHER
Access comprehensive regulatory information for Venous Blood Collection Kit, Professional Use in the European Union medical device market through Pure Global AI's free database. This Class A device is registered with EU EUDAMED under Primary DI 05056751600926 and manufactured by REAL Digital International Ltd in United Kingdom (ex Northern Ireland).
This page provides complete registration details including trade name (Venous Blood Collection Kit, Professional Use), manufacturer information, authorized representative details, competent authority (Ministerie van Volksgezondheid, Welzijn en Sport), 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.