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Nephrostomy / Drainage Set, Direct Puncture - EUDAMED Registration 08699158348861

Access comprehensive regulatory information for Nephrostomy / Drainage Set, Direct Puncture 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 08699158348861 and manufactured by GEOTEK MEDIKAL VE SAGLIK HIZMETLERI TIC.SAN.LTD.STI in Tรผrkiye.

This page provides complete registration details including trade name (Nephrostomy / Drainage Set, Direct Puncture), manufacturer information, competent authority (Turkish Medicine and Medical Devices Agency), 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
08699158348861
No
Nephrostomy / Drainage Set, Direct Puncture
Trade Name: Nephrostomy / Drainage Set, Direct Puncture
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Device Description (EMDN)

NEPHROSTOMY KITS, DIRECT PUNCTURE

Device Classification
Risk Class
Class IIa
CND Nomenclatures Code
U040201
Trade Name
Nephrostomy / Drainage Set, Direct Puncture
Implantable
No
Reusable
No
Measuring Function
No
Registration Information
Primary DI
08699158348861
Basic UDI
869915834GDPNU7
Version Date
June 24, 2024
Manufacturer Last Update
July 25, 2022
Active Status
No
Manufacturer
Country
Tรผrkiye
Country Type
EU_EXTENDED
Address
NO:12 IVEDIK OSB MAH AGAC METAL S.S. 1436 SK ANKARA
Email
info@geotekmedikal.com
Regulatory Information
Competent Authority
Turkish Medicine and Medical Devices Agency
Applicable Legislation
MDR (REGULATION (EU) 2017/745 on medical devices)
Placed On The Market
Tรผrkiye
Market Available
Tรผrkiye:None~None
Device Characteristics
Human Tissues
No
Animal Tissues
No