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TCO2 Quality Control - EUDAMED Registration 06947929500157

Access comprehensive regulatory information for TCO2 Quality Control in the European Union medical device market through Pure Global AI's free database. This Class A device is registered with EU EUDAMED under Primary DI 06947929500157 and manufactured by Meizhou Cornley Hi-Tech Co., Ltd. in China.

This page provides complete registration details including trade name (cornley), 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.

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EUDAMED Official Data
Class A
06947929500157
No
TCO2 Quality Control
Trade Name: cornley
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Device Description (EMDN)

BLOOD GAS ANALYSERS - CONSUMABLES

Device Classification
Risk Class
Class A
CND Nomenclatures Code
W0201040185
Trade Name
cornley
Implantable
No
Reusable
No
Measuring Function
No
Registration Information
Primary DI
06947929500157
Basic UDI
69479295AFT-TCO2QC9M
Version Date
November 29, 2023
Manufacturer Last Update
June 13, 2022
Active Status
No
Manufacturer
Country
China
Country Type
NON_EU
Address
Cornley Hi-Tech Industrial Park Jincheng Road, Fuda Hi-Tech Zone, Meixian Meizhou, Guangdong
Email
sales@cornley.com
Authorized Representative
SRN
DE-AR-000005946
Country
Germany
Address
71 NiederrheinstraรŸe Dรผsseldorf
Email
info@caretechion.de
Telephone
+49 211 2398900
Regulatory Information
Competent Authority
DE/CA20, Bezirksregierung Dรผsseldorf Dezernat 24
Applicable Legislation
IVDR (REGULATION (EU) 2017/746 on in vitro diagnostic medical devices)
Placed On The Market
Germany
Device Characteristics
Human Tissues
No
Animal Tissues
No