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K.H. Dewert GmbH

Germany DE-MF-000005967 Last updated 8 Jun 2026

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Devices
158
Registries
EUDAMED
FDA recalls
0

Catalogue158

Page 1 of 4

  • 900 Ref 900

    Class I EUDAMED Active
  • 2900 Ref 2900

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  • 108 Ref 108

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  • 2220XL/H Ref 2220XL/H

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  • 6070E Ref 6070E

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  • 6075E Ref 6075E

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  • 2645XLE Ref 2645XLE

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  • 6050E Ref 6050E

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  • 2830XLE Ref 2830XLE

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  • 2550XLE Ref 2550XLE

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  • 2115XLE Ref 2115XLE

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  • 2890XL/H Ref 2890XL/H

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  • 22 Ref 22

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  • 2114XLE Ref 2114XLE

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  • 61 Ref 61

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  • 2035XL/H Ref 2035XL/H

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  • 177 Ref 177

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  • 2105XLE Ref 2105XLE

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  • 36 Ref 36

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  • 2655XL/H Ref 2655XL/H

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  • 2011XLE Ref 2011XLE

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  • 119 Ref 119

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  • 2648XLE Ref 2648XLE

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  • 2114XL/H Ref 2114XL/H

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  • 2610XLE Ref 2610XLE

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  • 1050E Ref 1050E

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  • 2320XL/H Ref 2320XL/H

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  • 32 Ref 32

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  • 2895XLE Ref 2895XLE

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  • 2009XLE Ref 2009XLE

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  • 2030XLE Ref 2030XLE

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  • 109 Ref 109

    Class I EUDAMED Active
  • 4000E Ref 4000E

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  • 2860XLE Ref 2860XLE

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  • 2053XLE Ref 2053XLE

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  • 2804XL/H Ref 2804XL/H

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  • 2650XLE Ref 2650XLE

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  • 2656XLE Ref 2656XLE

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  • 2052XL/H Ref 2052XL/H

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  • 2006XL/H Ref 2006XL/H

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  • 2001XL/H Ref 2001XL/H

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  • 2650XL/H Ref 2650XL/H

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  • 4804E Ref 4804E

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  • 2815XL/H Ref 2815XL/H

    Class I EUDAMED Active
  • 2053XL/H Ref 2053XL/H

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  • 2550XL/H Ref 2550XL/H

    Class I EUDAMED Active
  • 2552XLE Ref 2552XLE

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  • 16 Ref 16

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  • 1090/H Ref 1090/H

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  • 6001E Ref 6001E

    Class I EUDAMED Active

Showing 1-50 of 158

About

We are your partner for practice and therapy facilities for hospitals, doctors and therapists. As a bedside specialist, we look forward to your wishes - Talk to us!

Translated from the manufacturer's own website. Source

What K.H. Dewert GmbH makes

K.H. Dewert GmbH manufactures a range of medical devices primarily used in clinical and therapeutic settings, including bedside diagnostic and treatment equipment. Their portfolio includes devices such as the 900 series for general medical use, the 2900 series for specialized diagnostic applications, and various models (e.g., 2220XL/H, 6070E) designed for precise measurements and therapeutic procedures. Additional products like the 2645XLE and 2890XL/H cater to specific clinical needs, such as extended functionality or enhanced performance in hospital environments.

The company’s devices are classified under Class I in the EU regulatory framework and are listed in the EUDAMED database. All products comply with relevant medical device directives and are intended for use within the European market. The manufacturer is based in Germany.

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

Information

Country
Germany
Address
7, Vollmestraße, Bielefeld, Germany
PRRC contact
Jörg Dewert
EUDAMED SRN
DE-MF-000005967