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Leica Microsystems CMS GmbH

Germany DE-MF-000019760 Last updated 23 Oct 2026

Devices
5
Registries
EUDAMEDFDA
FDA recalls
0

Catalogue5

  • DM2000 Led Ref 11888843

    Class A EUDAMED Active
  • DM1000 Led Ref 11888842

    Class A EUDAMED Active
  • DM2000 Ref 11888138

    Class A EUDAMED Active
  • DM2500 Ref 11888139

    Class A EUDAMED Active
  • DM1000 Ref 11888133

    Class A EUDAMED Active

What Leica Microsystems CMS GmbH makes

Leica Microsystems CMS GmbH manufactures microscopes, including models such as the DM2000 LED, DM1000 LED, DM2000, DM2500, and DM1000.

These devices are classified as Class A and are listed in the EUDAMED regulatory 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 does Leica Microsystems CMS GmbH manufacture?

Leica Microsystems CMS GmbH manufactures microscopes, including models such as the DM2000 LED, DM1000 LED, DM2000, DM2500, and DM1000. These devices are designed for various microscopy applications.

Where is Leica Microsystems CMS GmbH based?

Leica Microsystems CMS GmbH is based in Germany. The company operates from this location, where it designs and manufactures its microscope products for distribution to various markets.

Which regulatory registries list Leica Microsystems CMS GmbH's devices?

Leica Microsystems CMS GmbH's devices are listed in the EUDAMED regulatory registry. This registry is maintained by the European Union for medical devices, including the company's microscope models.

How are Leica Microsystems CMS GmbH's devices classified?

Leica Microsystems CMS GmbH's microscopes are classified as Class A medical devices. This classification indicates they present minimal potential risk to patients and users, typically requiring general controls rather than specialized regulatory controls.

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

Information

Country
Germany
Address
17-37, Ernst Leitz Straße, Wetzlar, Germany
Phone
0049 6441 292787
PRRC contact
Steffen Laabs
EUDAMED SRN
DE-MF-000019760
FDA FEI number
3003893952