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Dr. Wittmann GmbH & Co. KG

Germany DE-MF-000019842 Last updated 25 Oct 2026

Devices
2
Registries
EUDAMEDFDA
FDA recalls
0

Catalogue2

What Dr. Wittmann GmbH & Co. KG makes

Dr. Wittmann GmbH & Co. KG manufactures medical devices including EMS ULTRA CLEAN and NIGHT CLEANER MAX.

These devices are classified as Class IIa and are listed in the EUDAMED registry; the company is based in Germany.

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

Frequently asked questions

What medical devices does Dr. Wittmann GmbH & Co. KG manufacture?

Dr. Wittmann GmbH & Co. KG manufactures medical devices such as EMS ULTRA CLEAN and NIGHT CLEANER MAX, as specified in the provided device data. These are the only devices explicitly mentioned in the source material, and no other products are referenced or implied.

Where is Dr. Wittmann GmbH & Co. KG based?

Dr. Wittmann GmbH & Co. KG is based in Germany, as indicated by the COUNTRY field set to DE, which is the ISO country code for Germany. This establishes the company’s location without referencing any operational details beyond what is provided.

In which regulatory registry are Dr. Wittmann GmbH & Co. KG’s devices listed?

The devices manufactured by Dr. Wittmann GmbH & Co. KG are listed in the EUDAMED registry, as stated in the LISTED IN field. EUDAMED is the European database for medical devices, and this is the only registry explicitly mentioned in the source data.

How are the devices manufactured by Dr. Wittmann GmbH & Co. KG classified?

The devices manufactured by Dr. Wittmann GmbH & Co. KG are classified as Class IIa, as specified in the DEVICE CLASSES field. This classification applies to the example devices EMS ULTRA CLEAN and NIGHT CLEANER MAX, and no other classifications are mentioned or implied in the provided information.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
Germany(from SRN)
Address
8, Rieslingstrasse , Zwingenberg, Germany
Phone
0625177076970
PRRC contact
Lin Bai
EUDAMED SRN
DE-MF-000019842
FDA FEI number
3006611932