REBOA
- Risk class
- Class III
- CND nomenclatures code
- C0104020103
- Trade name
- REBOA
- Implantable
- No
- Reusable
- No
- Measuring function
- No
- Primary DI
- D-10887714022040NH
- Basic UDI
- B-10887714022040NH
- Version date
- February 17, 2023
- Manufacturer last update
- August 02, 2021
- Active status
- No
- Manufacturer name
- NuMED, Inc.
- Country
- United States
- Country type
- NON_EU
- Address
- 2880 Main Street Hopkinton
- nlaflesh@numedusa.com
- SRN
- NL-AR-000010437
- Country
- Netherlands
- Address
- 40 Hallenweg Best
- quality@heartmedical.nl
- Telephone
- +31499377388
- Competent authority
- Ministerie van Volksgezondheid, Welzijn en Sport
- Applicable legislation
- MDD (Directive 93/42/EEC on Medical Devices)
- Placed on the market
- Norway
- Market available
- Norway:2016-11-23~2024-05-24
- Human tissues
- No
- Animal tissues
- No
VASCULAR OCCLUSION CATHETERS
Access comprehensive regulatory information for REBOA in the European Union medical device market through Pure Global AI's free database. This Class III device is registered with EU EUDAMED under Primary DI D-10887714022040NH and manufactured by NuMED, Inc. in United States.
This page provides complete registration details including trade name (REBOA), 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.