EUDAMED registration 10888628043725NoKELLER FUNNEL
- Risk class
- Class IIa
- CND nomenclatures code
- P0680
- Trade name
- Keller Funnel 2
- Implantable
- No
- Reusable
- No
- Measuring function
- No
- Primary DI
- 10888628043725
- Basic UDI
- B-10888628043725
- Version date
- March 05, 2025
- Manufacturer last update
- November 21, 2024
- Active status
- No
- Manufacturer name
- Allergan Sales, LLC
- Country
- United States
- Country type
- NON_EU
- Address
- 2525 Dupont Drive Irvine, California
- customerservice@abbvie.com
- SRN
- EE-AR-000004308
- Country
- Estonia
- Address
- 30 Laki tn Tallinn
- enquiries@qualityfirstint.com
- Telephone
- +3726104196
- Competent authority
- Health Products Regulatory Authority, Medical Devices Department
- Applicable legislation
- MDD (Directive 93/42/EEC on Medical Devices)
- Placed on the market
- Ireland
- Market available
- Ireland:2013-08-06~None, United Kingdom (Northern Ireland only):2013-08-06~None, Spain:2013-08-06~None, France:2013-08-06~None, Sweden:2013-08-06~None, Norway:2013-08-06~None, Finland:2013-08-06~None, Portugal:2013-08-06~None
- Human tissues
- No
- Animal tissues
- No
BREAST IMPLANTS - ACCESSORIES
Access comprehensive regulatory information for KELLER FUNNEL in the European Union medical device market through Pure Global AI's free database. This Class IIa device is registered with EU EUDAMED under Primary DI 10888628043725 and manufactured by Allergan Sales, LLC in United States.
This page provides complete registration details including trade name (Keller Funnel 2), 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.