EU → North America Device Access

inomed Medizintechnik GmbH

DE-MF-000005589 · Germany · Emmendingen

inomed Medizintechnik GmbH is registered in the European database on medical devices as a manufacturer, with 184 devices declared. It is also registered as a device establishment with the U.S. FDA.

What this manufacturer declares

Class IIa183
Class I1

Most frequent device types declared: 230900, 505055, 520843, 540522, 590040.

Among these devices, 9 are declared sterile, 70 reusable, 3 active.

Devices declared under this manufacturer

Showing 12 of 184 declared devices.

Catalogue references include 230900, 520845, 540521, 540522, 801015, 803110.

European nomenclature codes declared: Z12100680, Z12109080, S010401, R01030201,Z12100480, N010180, S0199.

United States market access

FDA establishment registerRegistered with FDA
Matched entryINOMED MEDIZINTECHNIK GMBH (DE) · FDA 3004753785
Devices in EUDAMED184
Country of registrationGermany

Device-level evidence

Devices with a numeric GTIN184
Found in the U.S. device database65
Share35.3 %

Canadian market access

Health Canada licence listingLicensed in Canada
Matched entryINOMED MEDIZINTECHNIK GMBH

What it holds in Canada

Licences on record13
Currently active0
Class 2 devices13
First licensed2021-06-16

Licence types: Device Family (8), Single Device (2), Device Group Family (2), System (1).

Licensed under: C2 XPLORE, ALM TUBE, DELTA-ELECTRODE WITH STERILE CONNECTION CABLE, STIMULATION PROBE, LARYNGEAL ELECTRODE, PROBE.

North American profile: Both markets. inomed Medizintechnik GmbH is registered in both the United States and Canada.

Other manufacturers in Germany

All Germany manufacturers →