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Single-use Flexible Bronchoscope - EUDAMED Registration 06972197482744

Access comprehensive regulatory information for Single-use Flexible Bronchoscope 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 06972197482744 and manufactured by Hunan Vathin Medical Instrument 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.

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EUDAMED Official Data
Class IIa
06972197482744
Yes
Single-use Flexible Bronchoscope
EU EUDAMED Registered Medical Device
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Device Description (EMDN)

VIDEO BRONCHOSCOPES

Device Classification
Risk Class
Class IIa
CND Nomenclatures Code
Z12020802
Implantable
No
Reusable
No
Measuring Function
No
Registration Information
Primary DI
06972197482744
Basic UDI
697219748BC2X
Version Date
February 24, 2025
Manufacturer Last Update
November 15, 2022
Active Status
Yes
Manufacturer
Country
China
Country Type
NON_EU
Address
No 9 Chuanqi west road, Jiuhua Economic Development Zone Xiangtan
Email
service@vathin.com
Authorized Representative
SRN
NL-AR-000000121
Country
Netherlands
Address
Koningin Julianaplein 10, 1e Verd The Hague
Email
info@lotusnl.com
Regulatory Information
Competent Authority
Ministerie van Volksgezondheid, Welzijn en Sport
Applicable Legislation
MDR (REGULATION (EU) 2017/745 on medical devices)
Placed On The Market
Germany
Market Available
Germany:None~None
Device Characteristics
Human Tissues
No
Animal Tissues
No