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EUDAMED registration 06947929500850No

Electrolyte analyzer

Meizhou Cornley Hi-Tech Co., Ltd.Class AEU EUDAMEDTrade name: Cornley
VerifiedEUDAMED · official EU database
Device classification
Risk class
Class A
CND nomenclatures code
W0201040102
Trade name
Cornley
Implantable
No
Reusable
No
Measuring function
No
Registration information
Primary DI
06947929500850
Basic UDI
69479295AFT8R
Version date
November 29, 2023
Manufacturer last update
June 13, 2022
Active status
No
Manufacturer
Manufacturer name
Meizhou Cornley Hi-Tech Co., Ltd.
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
Name
Caretechion GmbH
SRN
DE-AR-000005946
Country
Germany
Address
71 Niederrheinstraße Düsseldorf
Email
info@caretechion.de
Telephone
+49 211 2398900
Regulatory information
Competent authority
DE/CA20, Bezirksregierung Düsseldorf 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
Device description (EMDN)

BLOOD GAS ANALYSERS - WITH ADDITIONAL PARAMETERS (pH, pO2, pCO2, Hct + metabolites + electrolytes, CO-oximeter parameters and coagulation parameters)

About this record

Access comprehensive regulatory information for Electrolyte analyzer 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 06947929500850 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 Düsseldorf 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.