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wenzhou dongfang medical instrument co., ltd

Country not established

Devices
17

Catalogue17

Newest first, rows 1-17 of 17

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  • Rhino Rescue KT-101

    None Registry: GUDID Class:I
  • Na 118

    None Registry: GUDID Class:I
  • N/A Kt-A05

    None Registry: GUDID Class:II
  • Na A01-C

    None Registry: GUDID Class:II
  • Na 01

    Withdrawn Registry: GUDID Class:II
  • Na Kt-GF03P

    None Registry: GUDID Class:I
  • N/A Kt-A02

    None Registry: GUDID Class:II
  • Na 01

    None Registry: GUDID Class:I
  • Na Kt-A011

    None Registry: GUDID Class:II
  • Na Kt-A23

    None Registry: GUDID Class:II
  • Lightning Products 01

    Withdrawn Registry: GUDID Class:II
  • Na 119

    None Registry: GUDID Class:I
  • Na Kt-A012

    None Registry: GUDID Class:II
  • Na Kt-A15

    None Registry: GUDID Class:II
  • Na 102

    None Registry: GUDID Class:I
  • N/A Kt-A02

    None Registry: GUDID Class:II
  • Na 01

    Withdrawn Registry: GUDID Class:I

Rows 1-17 of 17

Company details

DUNS number
529870243

Frequently asked questions

How many devices does wenzhou dongfang medical instrument co., ltd have in the registry?

The registry currently lists 17 devices for wenzhou dongfang medical instrument co., ltd. Devices recorded under merged duplicate company entries are counted once.

Which registries list wenzhou dongfang medical instrument co., ltd's devices?

Among its 17 most recently registered devices, wenzhou dongfang medical instrument co., ltd has devices listed in FDA GUDID (17 devices).

What risk classes do wenzhou dongfang medical instrument co., ltd's devices fall under?

Among its 17 most recently registered devices, the classes recorded for wenzhou dongfang medical instrument co., ltd's devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from wenzhou dongfang medical instrument co., ltd in the registry?

The most recently registered devices listed for wenzhou dongfang medical instrument co., ltd include Rhino Rescue KT-101, NA 118, N/A KT-A05 and NA A01-C.

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