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Shenzhen Bestman Instrument Co., Ltd.

China Last updated 8 Jun 2026

Devices
4
Registries
EUDAMEDFDA 510(k)
FDA recalls
0

Catalogue4

Authorised representatives

Frequently asked questions

How many devices does Shenzhen Bestman Instrument Co., Ltd. have in the registry?

The registry currently lists 4 devices for Shenzhen Bestman Instrument Co., Ltd.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Shenzhen Bestman Instrument Co., Ltd.'s devices?

Among its 4 most recently registered devices, Shenzhen Bestman Instrument Co., Ltd. has devices listed in EUDAMED (3 devices) and FDA 510(k) (2 devices). A device can be listed in more than one registry, so these counts overlap.

What risk classes do Shenzhen Bestman Instrument Co., Ltd.'s devices fall under?

Among its 4 most recently registered devices, the classes recorded for Shenzhen Bestman Instrument 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 Shenzhen Bestman Instrument Co., Ltd. in the registry?

The most recently registered devices listed for Shenzhen Bestman Instrument Co., Ltd. include Doppler FHR Detector (BF-500D+, BF-560), DOPPLER FETAL HEARTBEAT RATE DETECTOR, Fetal/Maternal Monitor (BFM-700M) and Vascular doppler detector.

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

Information

Address
8th floor, Yifang Building, No.315, Shuangming Avenue, Dongzhou Community, Guangming Street, Guangming District, Shenzhen, Guangdong, China, Shenzhen, China
Website
szbestman.com
PRRC contact
zhiqiang Chen
EUDAMED SRN
CN-MF-000031725