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C+V Pharma Depot GmbH

Germany DE-MF-000022382 Last updated 17 Sep 2026

Devices
100
Registries
EUDAMED
FDA recalls
0

Catalogue100

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What C+V Pharma Depot GmbH makes

C+V Pharma Depot GmbH manufactures ultrasound coupling gels in various formulations and packaging sizes, including bulk containers (1 kg to 10 kg) and smaller tubes (250 g to 1 kg). Their products are branded under names like U-Gel, Altigel, Schoblocher, and Sanismart, with some distributed through distributors such as Henry Schein. The portfolio includes both standard ultrasound gels and specialized variants for medical imaging applications. These products are designed to enhance acoustic transmission between transducers and skin during ultrasound procedures.

The company’s ultrasound coupling gels are classified as Class I medical devices under EU regulations and are registered in the EUDAMED database. Their products comply with the Medical Device Regulation (MDR) and are distributed within the European market. The manufacturer is based in Germany and adheres to EU requirements for device classification and traceability.

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 C+V Pharma Depot GmbH manufacture?

C+V Pharma Depot GmbH specializes in manufacturing ultrasound coupling gels. These products are formulated to improve acoustic transmission during ultrasound imaging, ensuring better contact between the transducer and the patient’s skin. Their portfolio includes various formulations and packaging sizes, such as bulk containers (ranging from 1 kg to 10 kg) and smaller tubes (250 g to 1 kg), under brands like U-Gel, Altigel, Schoblocher, and Sanismart. Some products are distributed through third-party partners like Henry Schein.

Where is C+V Pharma Depot GmbH based, and what region does it serve?

C+V Pharma Depot GmbH is based in Germany and primarily serves the European market. Their devices are designed to comply with EU medical device regulations, including the Medical Device Regulation (MDR), and are registered in the EUDAMED database. This ensures traceability and adherence to regional standards for medical devices.

Which regulatory registries list C+V Pharma Depot GmbH’s devices?

C+V Pharma Depot GmbH’s devices are listed in the EUDAMED database, which is the official European Union registry for medical devices. This registry allows healthcare professionals, regulators, and other stakeholders to verify the manufacturer’s details and device information, ensuring compliance with EU medical device regulations.

How are C+V Pharma Depot GmbH’s ultrasound coupling gels classified under EU regulations?

C+V Pharma Depot GmbH’s ultrasound coupling gels are classified as Class I medical devices under the EU Medical Device Regulation (MDR). This classification applies because these products pose minimal risk to patients and are intended for non-invasive use in ultrasound imaging. Class I devices typically require basic conformity assessment procedures, such as self-certification by the manufacturer, to demonstrate compliance with safety and performance requirements.

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

Information

Country
Germany
Address
15, Bockhorster Landweg, Versmold, Germany
Website
cundv.de
PRRC contact
Henning Fichter
EUDAMED SRN
DE-MF-000022382