Pure Global

Reusable Silicone Breathing Circuit - EUDAMED Registration 06957453025002

Access comprehensive regulatory information for Reusable Silicone Breathing Circuit 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 06957453025002 and manufactured by JINAN CHENSHENG in China.

This page provides complete registration details including 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.

Free Database
Powered by Pure Global AI
EUDAMED Official Data
Class IIa
06957453025002
No
Reusable Silicone Breathing Circuit
EU EUDAMED Registered Medical Device
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Device Description (EMDN)

RESPIRATORY CIRCUITS CONNECTION PIPES

Device Classification
Risk Class
Class IIa
CND Nomenclatures Code
R020301
Implantable
No
Reusable
Yes
Measuring Function
No
Registration Information
Primary DI
06957453025002
Basic UDI
695745300R020301001DA
Active Status
No
Manufacturer
Manufacturer Name
JINAN CHENSHENG
Country
China
Country Type
NON_EU
Address
No. 18-20,Lashan Road, Shizhong District Jinan
Email
jnchensheng@aliyun.com
Authorized Representative
SRN
DE-AR-000005110
Country
Germany
Address
1 Kochstr Willich
Email
info.m@luxuslw.de
Telephone
+49 1715605732
Regulatory Information
Competent Authority
DE/CA20, Bezirksregierung Dรผsseldorf Dezernat 24
Applicable Legislation
MDR (REGULATION (EU) 2017/745 on medical devices)
Placed On The Market
Germany
Market Available
Germany:None~None, United Kingdom (Northern Ireland only):None~None
Device Characteristics
Human Tissues
No
Animal Tissues
No