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Sotiria Mourkidou, M.D.

Country not established

Devices
1

What Sotiria Mourkidou, M.D. makes

The manufacturer produces single-use laryngoscope covers designed to reduce contamination risk during airway management procedures.

These devices are classified as Class I under FDA regulations and are listed via the 510(k) pathway. The manufacturer operates from the United States.

AI-generated from registry data, 2 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

  • Laryngoscope Cover Ref K945301

    Active Regimes: 510(k) Registry: 510(k) Class:I

Frequently asked questions

How many devices does Sotiria Mourkidou, M.D. have in the registry?

The registry currently lists 1 device for Sotiria Mourkidou, M.D.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Sotiria Mourkidou, M.D.'s devices?

Among its 1 most recently registered device, Sotiria Mourkidou, M.D. has devices listed in FDA 510(k) (1 device).

What risk classes do Sotiria Mourkidou, M.D.'s devices fall under?

Among its 1 most recently registered device, the classes recorded for Sotiria Mourkidou, M.D.'s devices are Class I. Each device page shows its own class and authorisation.

What are the newest devices from Sotiria Mourkidou, M.D. in the registry?

The most recently registered devices listed for Sotiria Mourkidou, M.D. include LARYNGOSCOPE COVER.

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