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Red drop Lab

Switzerland·CH-PR-000047258

Last updated May 23, 2026

What Red drop Lab makes

Red drop Lab manufactures medical devices designed for moisture management in healthcare settings, including systems like the DryCo and SmartCo. These products are intended to absorb and regulate moisture, likely targeting applications such as wound care, patient comfort, or surgical environments where fluid control is critical.

The company’s portfolio consists of Class IIa medical devices, which are regulated under EU medical device legislation. These devices are listed in the EU’s eudamed database, ensuring compliance with European Union requirements for traceability and regulatory transparency. The manufacturer is based in Switzerland.

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 Red drop Lab manufacture?

Red drop Lab specializes in medical devices focused on moisture management for healthcare applications. Their portfolio includes products like the DryCo and SmartCo, which are designed to absorb and regulate moisture. These devices are likely intended for use in environments where fluid control is essential, such as wound care, patient comfort, or surgical settings.

Where is Red drop Lab based?

Red drop Lab is headquartered in Switzerland (CH). The company’s location in Switzerland aligns with its focus on producing medical devices that comply with European Union regulatory standards.

Which regulatory registries list Red drop Lab’s devices?

Red drop Lab’s devices are listed in the eudamed database, which is the official EU registry for medical devices. This ensures transparency and traceability of their products under EU medical device regulations.

How are Red drop Lab’s devices classified under EU regulations?

Red drop Lab’s devices fall under Class IIa classification in the EU. This classification is determined based on their intended purpose and risk level, requiring compliance with specific EU Medical Device Regulation (MDR) requirements to ensure safety and performance.

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

Information

Country
Switzerland
Address
4, Chemin de Clamogne, Aubonne, Switzerland
LinkedIn
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Facebook
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Phone
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PRRC Contact
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EUDAMED SRN
CH-PR-000047258
FDA FEI Number
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DUNS Number
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Catalogue (7)

DeviceModel / ReferenceRegistriesClassStatus
Reddroplab DryCo RDL00_MICROBIOME
EUDAMED
Class IIaActive
Reddroplab DryCo RDL00_STI MICROBIOME
EUDAMED
Class IIaActive
Reddroplab SmartCo RDL01_STI
EUDAMED
Class IIaActive
Reddroplab SmartCo RDL01_MICROBIOME
EUDAMED
Class IIaActive
Reddroplab SmartCo RDL01_STI MICROBIOME
EUDAMED
Class IIaActive
Reddroplab DryCo RDL00_STI
EUDAMED
Class IIaActive
Reddroplab DryCo RDL00_STI_HH
EUDAMED
Class IIaActive

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