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Artificial teeth - EUDAMED Registration J017AW0M3L370

Access comprehensive regulatory information for Artificial teeth 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 J017AW0M3L370 and manufactured by VITA Zahnfabrik in Germany.

This page provides complete registration details including trade name (Neoversal®), manufacturer information, competent authority (DE/CA39, Regierungspräsidium Freiburg Referat 25), 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.

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EUDAMED Official Data
Class IIa
J017AW0M3L370
No
Artificial teeth
Trade Name: Neoversal®
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Device Description (EMDN)

MATERIALS FOR THE PREPARATION OF CUSTOM-MADE DENTAL DEVICES - OTHER

Device Classification
Risk Class
Class IIa
CND Nomenclatures Code
Q010699
Trade Name
Neoversal®
Implantable
No
Reusable
No
Measuring Function
No
Registration Information
Primary DI
J017AW0M3L370
Basic UDI
++J017AA2PG
Active Status
No
Manufacturer
Manufacturer Name
VITA Zahnfabrik
Country
Germany
Country Type
EU_MEMBER_STATE
Address
3. Spitalgasse Bad Säckingen
Email
Info@vita-zahnfabrik.com
Regulatory Information
Competent Authority
DE/CA39, Regierungspräsidium Freiburg Referat 25
Applicable Legislation
MDR (REGULATION (EU) 2017/745 on medical devices)
Placed On The Market
Germany
Market Available
Germany:2024-10-15~None
Device Characteristics
Human Tissues
No
Animal Tissues
No