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Ermis MedTech GmbH

Country not established FDA

Ermis MedTech GmbH is a medical device manufacturer, with 597 devices listed in FDA GUDID and EUDAMED (FDA Class II) as of 12 Nov 2026.

Devices
597
Registrations
FDA
FDA recalls
0

Registry facts

Counted by deviCERTS from registry records, 12 Nov 2026

Registries
  • FDA GUDID 597
  • EUDAMED 7

A device listed in two registries counts in both.

Device classes
  • FDA Class II 597
Identifiers
  • DUNS 313118522

At a glance

Counted by deviCERTS from registry records

Market reach

United States
FDA establishment

What Ermis MedTech GmbH makes

Ermis MedTech GmbH manufactures reusable device sterilization and disinfection containers designed for medical equipment processing. These containers are engineered to safely hold and sterilize reusable medical devices, ensuring compliance with infection control protocols in clinical settings.

The company’s products are classified as Class II medical devices under FDA regulations and are listed in the FDA’s Unique Device Identifier (UDI) database. The manufacturer operates from the United States.

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

Catalogue597

Newest first, rows 1-50 of 597

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Rows 1-50 of 597

Showing 1-50 of 597

Company details

DUNS number
313118522
Phone
+4974619648570

FDA establishments1

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

  • Ermis MedTech TUTTLINGEN Baden-Wurttemberg · DE FEI 3005071827

Frequently asked questions

How many devices does Ermis MedTech GmbH have in the registry?

The registry currently lists 597 devices for Ermis MedTech GmbH. Devices recorded under merged duplicate company entries are counted once.

Which registries list Ermis MedTech GmbH's devices?

Among its 50 most recently registered devices, Ermis MedTech GmbH has devices listed in FDA GUDID (50 devices).

What risk classes do Ermis MedTech GmbH's devices fall under?

Among its 50 most recently registered devices, the classes recorded for Ermis MedTech GmbH's devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Ermis MedTech GmbH in the registry?

The most recently registered devices listed for Ermis MedTech GmbH include ERMIS ER804.090, ERMIS ER800.020, ERMIS ER802.000 and ERMIS ER802.020.

Which FDA establishments are linked to Ermis MedTech GmbH?

1 FDA establishment is linked to Ermis MedTech GmbH in the registry; they are listed on the company page.

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