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Ze Fang Technology Co., Ltd.

Active in EUDAMED

Taiwanfrom SRN EUDAMED FDA SRN TW-MF-000016035 FEI 3013689189

Devices
667
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.
MedNet EC-REP GmbHDE

What Ze Fang Technology Co., Ltd. makes

Ze Fang Technology Co., Ltd. manufactures orthodontic tubes, including the L1-M-002212 and Mico one models.

The company is based in Taiwan, and its portfolio consists of Class IIa medical devices that are listed in EUDAMED.

AI-generated from registry data, 4 Oct 2026. Not verified by deviCERTS or the manufacturer.

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Company details

EUDAMED SRN
TW-MF-000016035
FDA FEI number
3013689189
DUNS number
656214227
EU VAT number
24630295
EUDAMED status
Active
EUDAMED registered name
Ze Fang Technology Co., Ltd.
Registered address
1F, No.17, Alley. 81, Lane. 2, Zhongxing Rd., Sec.1, Ruicheng Li, Dali Dist, 412, Taichung, Taiwan
PRRC contact
Kun Sian Lin(public in EUDAMED)

Frequently asked questions

How many devices does ZE FANG TECHNOLOGY CO., LTD. have in the registry?

The registry currently lists 667 devices for ZE FANG TECHNOLOGY CO., LTD.. Devices recorded under merged duplicate company entries are counted once.

Which registries list ZE FANG TECHNOLOGY CO., LTD.'s devices?

Among its 50 most recently registered devices, ZE FANG TECHNOLOGY CO., LTD. has devices listed in FDA GUDID (50 devices).

What risk classes do ZE FANG TECHNOLOGY CO., LTD.'s devices fall under?

Among its 50 most recently registered devices, the classes recorded for ZE FANG TECHNOLOGY CO., LTD.'s devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from ZE FANG TECHNOLOGY CO., LTD. in the registry?

The most recently registered devices listed for ZE FANG TECHNOLOGY CO., LTD. include Mico One Orthodontic Screw F1-AS-211507, Mico One Orthodontic Screw F1-AS-411507, Mico One Orthodontic Screw F1-AS-421507 and Mico One Orthodontic Screw F1-AS-221507.

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