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EUDAMED registration 06975202773035Yes

Monitor for Single-Use Endoscopy

Hunan Endoso Life Technology Co., LtdClass IIaEU EUDAMEDTrade name: Monitor for Single-Use Endoscopy
VerifiedEUDAMED · official EU database
Device classification
Risk class
Class IIa
CND nomenclatures code
Z12020406
Trade name
Monitor for Single-Use Endoscopy
Implantable
No
Reusable
Yes
Measuring function
No
Registration information
Primary DI
06975202773035
Basic UDI
697520277010HY
Version date
January 24, 2025
Manufacturer last update
March 14, 2022
Active status
Yes
Manufacturer
Country
China
Country type
NON_EU
Address
Fourth floor of building 10 Innovation and entrepreneurship center, No. 31, Dongfeng Road, Heping Street, economic and Technological Development Zone Xiangtan City, Hunan Province
Email
wangfu@endoso.com.cn
Authorized representative
SRN
NL-AR-000000444
Country
Netherlands
Address
Treubstraat 1 Rijswijk
Email
ar@umedwings.eu
Telephone
+31 (0) 642758955
Regulatory information
Competent authority
Ministerie van Volksgezondheid, Welzijn en Sport
Applicable legislation
MDR (REGULATION (EU) 2017/745 on medical devices)
Placed on the market
Netherlands
Market available
Netherlands:2025-01-06~2025-01-24
Device characteristics
Human tissues
No
Animal tissues
No
Device description (EMDN)

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About this record

Access comprehensive regulatory information for Monitor for Single-Use Endoscopy 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 06975202773035 and manufactured by Hunan Endoso Life Technology Co., Ltd in China.

This page provides complete registration details including trade name (Monitor for Single-Use Endoscopy), 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.