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Dragerwerk AG

FDA registration: United States Last updated 23 May 2026

Devices
699
Registries
GUDIDEUDAMEDFDA 510(k)
FDA recalls
0

Catalogue699

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Showing 651-699 of 699

What Dragerwerk AG makes

Dragerwerk AG manufactures medical equipment including oxymeters and the Incubator 8000 and Incubator 8000 IC models.

These devices are classified as Class II medical products and are listed in the FDA 510(k) registry, with the company maintaining operations in the US.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Information

FDA registration
United States(from the FDA device records)