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Nanjing Nuoyuan Medical Devices Co., Ltd

Active in EUDAMED

Chinafrom SRN EUDAMED SRN CN-MF-000036076

Devices
2
Registrations
EUDAMED

At a glance

Counted by deviCERTS from registry records

Market reach

European Union
EUDAMED actor

What Nanjing Nuoyuan Medical Devices Co., Ltd makes

Nanjing Nuoyuan Medical Devices Co., Ltd manufactures 4K endoscopic fluorescent imaging systems. These devices are designed for medical imaging and endoscopic procedures.

The company is based in China. Its products are classified as Class IIa medical devices and are listed in the EUDAMED database.

AI-generated from registry data, 20 Sep 2026. Not verified by deviCERTS or the manufacturer.

Catalogue2

Newest first, rows 1-2 of 2

Company details

EUDAMED SRN
CN-MF-000036076
EUDAMED status
Active
EUDAMED registered name
Nanjing Nuoyuan Medical Devices Co.,Ltd
Registered address
No.18, Fuqian South Road, Nanjing Fourth Bridge Economic Zone, Longpao Street, Liuhe District,, 211514, Nanjing,Jiangsu, China
PRRC contact
Liyang Xia(public in EUDAMED)

Frequently asked questions

How many devices does Nanjing Nuoyuan Medical Devices Co., Ltd have in the registry?

The registry currently lists 2 devices for Nanjing Nuoyuan Medical Devices Co., Ltd. Devices recorded under merged duplicate company entries are counted once.

Which registries list Nanjing Nuoyuan Medical Devices Co., Ltd's devices?

Among its 2 most recently registered devices, Nanjing Nuoyuan Medical Devices Co., Ltd has devices listed in EUDAMED (2 devices).

What risk classes do Nanjing Nuoyuan Medical Devices Co., Ltd's devices fall under?

Among its 2 most recently registered devices, the classes recorded for Nanjing Nuoyuan Medical Devices Co., Ltd's devices are Class IIa. Each device page shows its own class and authorisation.

What are the newest devices from Nanjing Nuoyuan Medical Devices Co., Ltd in the registry?

The most recently registered devices listed for Nanjing Nuoyuan Medical Devices Co., Ltd include 4K Endoscopic Fluorescent Imaging System.

Generated automatically from registry data and not verified by a human reviewer.