Single-Use Digital Flexible Ureteroscope
- Risk class
- Class IIa
- CND nomenclatures code
- Z12020705
- Trade name
- Single-Use Digital Flexible Ureteroscope
- Implantable
- No
- Reusable
- No
- Measuring function
- No
- Primary DI
- 06975202772922
- Basic UDI
- 697520277008JD
- Version date
- January 24, 2025
- Manufacturer last update
- March 14, 2022
- Active status
- Yes
- Manufacturer name
- Hunan Endoso Life Technology Co., Ltd
- 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
- wangfu@endoso.com.cn
- SRN
- NL-AR-000000444
- Country
- Netherlands
- Address
- Treubstraat 1 Rijswijk
- ar@umedwings.eu
- Telephone
- +31 (0) 642758955
- 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:2024-12-26~2025-01-27
- Human tissues
- No
- Animal tissues
- No
NEPHROSCOPES
Access comprehensive regulatory information for Single-Use Digital Flexible Ureteroscope 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 06975202772922 and manufactured by Hunan Endoso Life Technology Co., Ltd in China.
This page provides complete registration details including trade name (Single-Use Digital Flexible Ureteroscope), 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.