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Cheek Retractor - EUDAMED Registration 06977449600020

Access comprehensive regulatory information for Cheek Retractor 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 06977449600020 and manufactured by Anhui Huming Medical Technology Co., Ltd in China.

This page provides complete registration details including manufacturer information, authorized representative details, competent authority (DE/CA20, Bezirksregierung Düsseldorf Dezernat 24), 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
06977449600020
No
Cheek Retractor
EU EUDAMED Registered Medical Device
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Device Description (EMDN)

NON-SPECIALIST SURGICAL INSTRUMENTS AND KITS, SINGLE-USE

Device Classification
Risk Class
Class I
CND Nomenclatures Code
V9012
Implantable
No
Reusable
No
Measuring Function
No
Registration Information
Primary DI
06977449600020
Basic UDI
6977449600020EY
Version Date
July 23, 2024
Manufacturer Last Update
June 28, 2024
Active Status
No
Manufacturer
Country
China
Country Type
NON_EU
Address
No. 336, Tianhe Road, Luyang Industrial Zone, Luyang District Hefei City, Anhui Province
Email
171275846@qq.com
Authorized Representative
SRN
DE-AR-000023447
Country
Germany
Address
8 Gneisenaustraße Düsseldorf
Email
eurep@humiss.com
Telephone
+49-211-90760042
Regulatory Information
Competent Authority
DE/CA20, Bezirksregierung Düsseldorf Dezernat 24
Applicable Legislation
MDR (REGULATION (EU) 2017/745 on medical devices)
Placed On The Market
Germany
Device Characteristics
Human Tissues
No
Animal Tissues
No