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Dental Prophylaxis Powder - EUDAMED Registration 06971560453480

Access comprehensive regulatory information for Dental Prophylaxis Powder 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 06971560453480 and manufactured by Guilin Refine Medical Instrument Co.,Ltd. in China.

This page provides complete registration details including trade name (Dental Prophylaxis Powder), manufacturer information, authorized representative details, competent authority (DE/CA22 - Bezirksregierung Mรผnster), 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 I
06971560453480
No
Dental Prophylaxis Powder
Trade Name: Dental Prophylaxis Powder
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Device Description (EMDN)

DENTAL ABRASIVE AND POLISHING MATERIALS

Device Classification
Risk Class
Class I
CND Nomenclatures Code
Q01010403
Trade Name
Dental Prophylaxis Powder
Implantable
No
Reusable
No
Measuring Function
No
Registration Information
Primary DI
06971560453480
Basic UDI
697156045SBPSJ
Version Date
October 08, 2024
Manufacturer Last Update
June 12, 2024
Active Status
No
Manufacturer
Country
China
Country Type
NON_EU
Address
No.8-3 Information Industrial Park, High-Tech Zone, Qixing District Guilin,Guangxi
Email
refine@refine-med.com
Authorized Representative
SRN
DE-AR-000011194
Country
Germany
Address
10 Borkstrasse Mรผnster
Email
contact@mednet-ecrep.com
Regulatory Information
Competent Authority
DE/CA22 - Bezirksregierung Mรผnster
Applicable Legislation
MDR (REGULATION (EU) 2017/745 on medical devices)
Placed On The Market
Germany
Market Available
Germany:None~None
Device Characteristics
Human Tissues
No
Animal Tissues
No