EUDAMED registration 08906155700500No

Percutaneous Nephrostomy Drainage Catheter & Set

Name: Percutaneous Nephrostomy Drainage Catheter & Set — EUDAMED registration 08906155700500
Creator: MANISH MEDI INNOVATION PRIVATE LIMITED
Keywords: Percutaneous Nephrostomy Drainage Catheter & Set , 08906155700500, UROMED, Class IIa, MANISH MEDI INNOVATION PRIVATE LIMITED, EUDAMED registration

MANISH MEDI INNOVATION PRIVATE LIMITEDClass IIaEU EUDAMEDTrade name: UROMED

VerifiedEUDAMED · official EU database

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

Manufacturer name: MANISH MEDI INNOVATION PRIVATE LIMITED
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

Name: CMC Medical Devices & Drugs SL
SRN: ES-AR-000000293
Country: Spain
Address: C/ Horacio Lengo N18 Málaga
Email: info@cmcmedicaldevices.com
Telephone: +34951214054

Regulatory information

Competent authority: Agencia Española de Medicamentos y Productos Sanitarios
Applicable legislation: MDR (REGULATION (EU) 2017/745 on medical devices)
Placed on the market: Türkiye
Market available: Türkiye:2021-05-21~2029-05-26

Device characteristics

Human tissues: No
Animal tissues: No

Device description (EMDN)

NEPHROSTOMY KITS, SELDINGER METHOD

About this record

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 Española 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.