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Xi'an Furuize Biotechnology Co., Ltd.

Active in EUDAMED

Chinafrom SRN EUDAMED FDA SRN CN-MF-000026472 FEI 3016171962

Devices
3
Registrations
EUDAMEDFDA
FDA recalls
0

At a glance

Counted by deviCERTS from registry records

Market reach

European Union
EUDAMED actor
United States
FDA FEI
Authorised rep.
Humiss Beratung GmbHDE

Catalogue3

Company details

EUDAMED SRN
CN-MF-000026472
FDA FEI number
3016171962
EUDAMED status
Active
EUDAMED registered name
Xi'an Furuize Biotechnology Co., Ltd.
EUDAMED abbreviated name
Furuize
Registered address
Room 11131, Building 3, i Duhui, No. 11, Tangyan South Road, Zhangba Street Office, High-Tech Zone, 710065, Xi'an, China
Phone
+86-13389223500
PRRC contact
Frank Wang(public in EUDAMED)

What Xi'an Furuize Biotechnology Co., Ltd. makes

Xi'an Furuize Biotechnology Co., Ltd. manufactures menstrual cups.

The company is based in China, and its products are classified as Class I medical devices. These devices are listed in the EUDAMED database.

AI-generated from registry data, 5 Oct 2026. Not verified by deviCERTS or the manufacturer.

Frequently asked questions

How many devices does Xi'an Furuize Biotechnology Co., Ltd. have in the registry?

The registry currently lists 3 devices for Xi'an Furuize Biotechnology Co., Ltd.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Xi'an Furuize Biotechnology Co., Ltd.'s devices?

Among its 3 most recently registered devices, Xi'an Furuize Biotechnology Co., Ltd. has devices listed in EUDAMED (3 devices).

What risk classes do Xi'an Furuize Biotechnology Co., Ltd.'s devices fall under?

Among its 3 most recently registered devices, the classes recorded for Xi'an Furuize Biotechnology Co., Ltd.'s devices are Class I. Each device page shows its own class and authorisation.

What are the newest devices from Xi'an Furuize Biotechnology Co., Ltd. in the registry?

The most recently registered devices listed for Xi'an Furuize Biotechnology Co., Ltd. include Menstrual Cup.

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