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Ureteral Stents - EUDAMED Registration 06974269820010

Access comprehensive regulatory information for Ureteral Stents 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 06974269820010 and manufactured by Baihe Medical Technology (Wuhan) Co., Ltd. in China.

This page provides complete registration details including trade name (Ureteral Stents), manufacturer information, authorized representative details, competent authority (DE/CA20, Bezirksregierung Dรผsseldorf 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 IIa
06974269820010
No
Ureteral Stents
Trade Name: Ureteral Stents
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Device Description (EMDN)

DOUBLE LOOP URETERAL STENTS

Device Classification
Risk Class
Class IIa
CND Nomenclatures Code
U020302
Trade Name
Ureteral Stents
Implantable
No
Reusable
No
Measuring Function
No
Registration Information
Primary DI
06974269820010
Basic UDI
697426982US01SK
Version Date
September 27, 2022
Manufacturer Last Update
July 08, 2022
Active Status
No
Manufacturer
Country
China
Country Type
NON_EU
Address
No.118 Golden Road West Xiantao
Email
whhklxmm@sina.com
Authorized Representative
SRN
DE-AR-000005133
Country
Germany
Address
83 Heerdter Lohweg Dรผsseldorf
Email
eu-rep@share-info.com
Regulatory Information
Competent Authority
DE/CA20, Bezirksregierung Dรผsseldorf Dezernat 24
Applicable Legislation
MDR (REGULATION (EU) 2017/745 on medical devices)
Placed On The Market
Ireland
Market Available
Ireland:2024-08-16~2039-12-31, United Kingdom (Northern Ireland only):2024-08-16~2039-12-31
Device Characteristics
Human Tissues
No
Animal Tissues
No