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EUDAMED registration 06974222260631No

Sperm DNA Fragmentation Detection Kit (Sperm Chromatin Dispersion Method)

Zhuhai Cariad Medical Technology Co., Ltd.Class AEU EUDAMED
VerifiedEUDAMED · official EU database
Device classification
Risk class
Class A
CND nomenclatures code
W01030708
Implantable
No
Reusable
No
Measuring function
No
Registration information
Primary DI
06974222260631
Basic UDI
697422226019GX
Active status
No
Manufacturer
Manufacturer name
Zhuhai Cariad Medical Technology Co., Ltd.
Country
China
Country type
NON_EU
Address
5/F, Block 6, No.6 Jinyuan 1st Rd., High-tech Zone, 519085 Zhuhai, Guangdong, P. R. China Zhuhai
Email
support@cariad.com.cn
Authorized representative
Name
PureCE B.V.
SRN
NL-AR-000006069
Country
Netherlands
Address
13 Distriebutieweg Waddinxveen
Email
info@purece.nl
Telephone
+31 10 899 0449
Regulatory information
Competent authority
Ministerie van Volksgezondheid, Welzijn en Sport
Applicable legislation
IVDR (REGULATION (EU) 2017/746 on in vitro diagnostic medical devices)
Placed on the market
Greece
Device characteristics
Human tissues
No
Animal tissues
No
Device description (EMDN)

STAIN SOLUTIONS (HISTOLOGY/CYTOLOGY)

About this record

Access comprehensive regulatory information for Sperm DNA Fragmentation Detection Kit (Sperm Chromatin Dispersion Method) 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 06974222260631 and manufactured by Zhuhai Cariad Medical Technology Co., Ltd. in China.

This page provides complete registration details including manufacturer information, authorized representative details, competent authority (Ministerie van Volksgezondheid, Welzijn en Sport), 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.