EU → North America Device Access

GETSCH+HILLER Medizintechnik GmbH

DE-MF-000007007 · Germany · Tuttlingen

GETSCH+HILLER Medizintechnik GmbH is registered in the European database on medical devices as a manufacturer, with 855 devices declared. It is also registered as a device establishment with the U.S. FDA.

What this manufacturer declares

Class IIb591
Class IIa264

Most frequent device types declared: Container und Siebkörbe, Forceps, Grasper, Grasping Forceps, Handle.

Among these devices, 3 are declared sterile, 798 reusable, 589 active.

Devices declared under this manufacturer

Showing 12 of 855 declared devices.

Catalogue references include 30-30021.60, 30-50001.22, 30-50001.45, 30-50002.45, 30-50011.25, 36-09112.33UZ.

European nomenclature codes declared: L1299, L020801, L99, L0205, S010401, S010499.

United States market access

FDA establishment registerRegistered with FDA
Matched entryGETSCH + HILLER MEDIZINTECHNIK GMBH (DE) · FDA 3008911114
Devices in EUDAMED855
Country of registrationGermany

Device-level evidence

Devices with a numeric GTIN855
Found in the U.S. device database0
Share0.0 %

Canadian market access

Health Canada licence listingNot found in the Canadian register

⚠️ Canada lists no Class I devices at all — what that excludes.

North American profile: United States only. GETSCH+HILLER Medizintechnik GmbH is registered in the United States but was not found in the Canadian register.

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