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Hangzhou IVISTA Medical Devices Co., Ltd.

Active in EUDAMED

Chinafrom SRN EUDAMED SRN CN-MF-000034899

Devices
13
Registrations
EUDAMED

At a glance

Counted by deviCERTS from registry records

Market reach

European Union
EUDAMED actor
Authorised rep.
MedPath GmbHDE

Catalogue13

Newest first, rows 1-13 of 13

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Rows 1-13 of 13

Company details

EUDAMED SRN
CN-MF-000034899
DUNS number
699364781
EUDAMED status
Active
EUDAMED registered name
Hangzhou IVISTA Medical Devices Co., Ltd.
Registered address
1st Floor, No. 7 Chunjiang Road, Qiaonan Block, Xiaoshan Economic and Technological Development Zone, Ningwei Sub-district, Xiaoshan District, Hangzhou City, China (Zhejiang) Pilot Free Trade Zone 311215, China, 311215, Hangzhou City, Zhejiang Province, China
PRRC contact
Yao Cheng(public in EUDAMED)

Frequently asked questions

How many devices does Hangzhou IVISTA Medical Devices Co., Ltd. have in the registry?

The registry currently lists 13 devices for Hangzhou IVISTA Medical Devices Co., Ltd.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Hangzhou IVISTA Medical Devices Co., Ltd.'s devices?

Among its 13 most recently registered devices, Hangzhou IVISTA Medical Devices Co., Ltd. has devices listed in EUDAMED (1 device), FDA 510(k) (1 device) and FDA GUDID (12 devices). A device can be listed in more than one registry, so these counts overlap.

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

Among its 13 most recently registered devices, the classes recorded for Hangzhou IVISTA Medical Devices Co., Ltd.'s devices are Class IIa and Class II. Each device page shows its own class and authorisation.

What are the newest devices from Hangzhou IVISTA Medical Devices Co., Ltd. in the registry?

The most recently registered devices listed for Hangzhou IVISTA Medical Devices Co., Ltd. include ZIRCONIA BLOCK ST-5M3-D98*18, ZIRCONIA BLOCK ST-5M3-D98*20, ZIRCONIA BLOCK 3D-5M3-AG*22 and ZIRCONIA BLOCK 3D-5M3-AG*25.

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