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Percutaneous Nephrostomy Drainage Catheter & Set - EUDAMED Registration 08906155700500

Access comprehensive regulatory information for Percutaneous Nephrostomy Drainage Catheter & Set 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 08906155700500 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
08906155700500
No
Percutaneous Nephrostomy Drainage Catheter & Set
Trade Name: UROMED
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Device Description (EMDN)

NEPHROSTOMY KITS, SELDINGER METHOD

Device Classification
Risk Class
Class IIa
CND Nomenclatures Code
U040202
Trade Name
UROMED
Implantable
No
Reusable
No
Measuring Function
No
Registration Information
Primary DI
08906155700500
Basic UDI
890615570PCNSLT
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:2021-05-21~2029-05-26
Device Characteristics
Human Tissues
No
Animal Tissues
No