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Boen Healthcare Co., Ltd

Active in EUDAMED

Chinafrom SRN EUDAMED FDA SRN CN-MF-000040773 FEI 3045058049

Devices
165
Registrations
EUDAMEDFDA
FDA recalls
0

At a glance

Counted by deviCERTS from registry records

Market reach

European Union
EUDAMED actor
United States
FDA establishment

Catalogue165

Newest first, rows 1-50 of 165

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Rows 1-50 of 165

Showing 1-50 of 165

Company details

EUDAMED SRN
CN-MF-000040773
FDA FEI number
3045058049
EUDAMED status
Active
EUDAMED registered name
Boen Healthcare Co.,Ltd
Registered address
No. 8, Unit 408, Building T2,, 215127, Suzhou, China
PRRC contact
Jing Zhu(public in EUDAMED)

FDA establishments1

Registered with the FDA under this company group, matched by name.

  • Boen Healthcare Co., Ltd. US

From the company website

Read 18 Sep 2026

BOENMED manufacturing innovative, safe, high quality and competitive medical, surgical and laboratory products.

From the manufacturer's own website. Source

Frequently asked questions

How many devices does Boen Healthcare Co.,Ltd have in the registry?

The registry currently lists 165 devices for Boen Healthcare Co.,Ltd. Devices recorded under merged duplicate company entries are counted once.

Which registries list Boen Healthcare Co.,Ltd's devices?

Among its 50 most recently registered devices, Boen Healthcare Co.,Ltd has devices listed in EUDAMED (50 devices).

What risk classes do Boen Healthcare Co.,Ltd's devices fall under?

Among its 50 most recently registered devices, the classes recorded for Boen Healthcare Co.,Ltd's devices are Class I and IVDR Class A. Each device page shows its own class and authorisation.

What are the newest devices from Boen Healthcare Co.,Ltd in the registry?

The most recently registered devices listed for Boen Healthcare Co.,Ltd include Cohesive Bandage, Plastic test tube, Sports Tape and TaiYi Moxa Rolls.

Which FDA establishments are linked to Boen Healthcare Co.,Ltd?

1 FDA establishment is linked to Boen Healthcare Co.,Ltd in the registry; they are listed on the company page.

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