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Biliary Stent - EUDAMED Registration 08906155705406

Access comprehensive regulatory information for Biliary Stent 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 08906155705406 and manufactured by MANISH MEDI INNOVATION PRIVATE LIMITED in India.

This page provides complete registration details including trade name (UROMED), manufacturer information, authorized representative details, competent authority (Agencia Espaรฑola de Medicamentos y Productos Sanitarios), 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
08906155705406
No
Biliary Stent
Trade Name: UROMED
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Device Description (EMDN)

BILIARY TUBES

Device Classification
Risk Class
Class IIa
CND Nomenclatures Code
G03040301
Trade Name
UROMED
Implantable
No
Reusable
No
Measuring Function
No
Registration Information
Primary DI
08906155705406
Basic UDI
890615570BSY8
Version Date
February 10, 2025
Manufacturer Last Update
March 01, 2024
Active Status
No
Manufacturer
Country
India
Country Type
NON_EU
Address
SY NO. 150/2,No.53,54,55,68,69,70, Bannerghatta Main Road, ABT Layout, Hullahalli village, CK Palya, Bannerghatta, Bengaluru, Bengaluru(Urban),Karnataka, 560083 560083 Bangalore
Email
nirmalkm1979@gmail.com
Authorized Representative
SRN
ES-AR-000000293
Country
Spain
Address
C/ Horacio Lengo N18 Mรกlaga
Email
info@cmcmedicaldevices.com
Telephone
+34951214054
Regulatory Information
Competent Authority
Agencia Espaรฑola de Medicamentos y Productos Sanitarios
Applicable Legislation
MDR (REGULATION (EU) 2017/745 on medical devices)
Placed On The Market
Tรผrkiye
Market Available
Tรผrkiye:2020-01-01~2029-12-31
Device Characteristics
Human Tissues
No
Animal Tissues
No