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SuZhou Emy Medical Supplies Co., Ltd.

Country not established FDA

Part of Suzhou Emy Medical Supplies Co., Ltd.

Devices
1
Registrations
FDA
FDA recalls
0

At a glance

Counted by deviCERTS from registry records

Market reach

United States
FDA establishment

What SuZhou Emy Medical Supplies Co., Ltd. makes

SuZhou Emy Medical Supplies Co., Ltd. manufactures general-purpose medical fibre padding, including the Emyms product line.

The company's devices are classified as Class I and are listed in the FDA UDI registry. The company is based in the US.

AI-generated from registry data, 20 Sep 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

Company details

DUNS number
421272935

FDA establishments1

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

  • Suzhou Emy Medical Supplies Co., Ltd. ChangShu Jiangsu · CN FEI 3009290468

Frequently asked questions

How many devices does SuZhou Emy Medical Supplies Co., Ltd. have in the registry?

The registry currently lists 1 device for SuZhou Emy Medical Supplies Co., Ltd.. Devices recorded under merged duplicate company entries are counted once.

Which registries list SuZhou Emy Medical Supplies Co., Ltd.'s devices?

Among its 1 most recently registered device, SuZhou Emy Medical Supplies Co., Ltd. has devices listed in FDA GUDID (1 device).

What risk classes do SuZhou Emy Medical Supplies Co., Ltd.'s devices fall under?

Among its 1 most recently registered device, the classes recorded for SuZhou Emy Medical Supplies Co., Ltd.'s devices are Class I. Each device page shows its own class and authorisation.

What are the newest devices from SuZhou Emy Medical Supplies Co., Ltd. in the registry?

The most recently registered devices listed for SuZhou Emy Medical Supplies Co., Ltd. include Emyms 10cmx3m.

Which FDA establishments are linked to SuZhou Emy Medical Supplies Co., Ltd.?

1 FDA establishment is linked to SuZhou Emy Medical Supplies Co., Ltd. in the registry; they are listed on the company page.

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