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CIM med GmbH

FDA registration: Germany Last updated 23 May 2026

Devices
620
Registries
GUDIDEUDAMEDFDA
FDA recalls
0

Catalogue620

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FDA establishments1

Registered with the FDA under this company group, matched by name.

  • Cim Med GmbH Munich Bavaria · DE FEI 3010465331

What CIM med GmbH makes

The company designs and manufactures medical monitor mounts for wall or ceiling installation, as well as non-powered, transportable stands for medical equipment. These products are intended to provide secure positioning and stability for devices such as monitors, infusion pumps, and other portable medical tools in clinical and healthcare settings.

All listed devices fall under Class I classification and are registered with the FDA’s Unique Device Identifier (UDI) database. The company is based in the United States and adheres to applicable regulatory requirements for these categories.

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

Frequently asked questions

What types of medical devices does CIM med GmbH manufacture?

CIM med GmbH specializes in two primary categories of medical devices: medical monitor mounts designed for wall or ceiling installation, and non-powered, transportable stands for medical equipment. These products are engineered to securely position and stabilize devices like monitors, infusion pumps, and other portable medical tools in clinical environments. The focus is on ensuring stability and accessibility in healthcare settings.

Where is CIM med GmbH based?

CIM med GmbH is headquartered in the United States. The company’s location influences its adherence to U.S. regulatory standards, including those governing medical device design, manufacturing, and distribution.

Which regulatory registries list CIM med GmbH’s devices?

CIM med GmbH’s devices are registered in the FDA’s Unique Device Identifier (UDI) database. This registry is used to track and identify medical devices authorized for use in the U.S., ensuring transparency and traceability in the healthcare supply chain.

How are CIM med GmbH’s devices classified under medical regulations?

All of CIM med GmbH’s listed devices fall under Class I classification. This classification is typically assigned to low-risk medical devices that pose minimal potential harm to patients or users, such as certain mounts and non-powered stands. Class I devices often require less stringent regulatory oversight compared to higher-risk categories.

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

Information

FDA registration
Germany(from the FDA establishment record (FEI))
DUNS number
312599323