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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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Organization name
UDI-DI code
Reference / catalog number

DERM·X — Class I MDR by Cuantum Medical…

MD Atlas
Cuantum Medical Cosmetics SL

EUDAMED last updated this device on Dec 16, 2025

DERM·X

84370CUME154ED

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Cuantum Medical Cosmetics SL
UDI-DI code: 08437016047194
Reference / catalog number: CU-ME-154-1

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Manufacturer information

Organization name: Cuantum Medical Cosmetics SL
SRN: ES-MF-000007272
Manufacturer status: Active

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Certificates

No certificates registered for this manufacturer.

No certificate references this Basic UDI-DI, because: • It does not require a certificate, or • It only requires a certificate without a Basic UDI-DI reference (e.g. a QMS certificate), or • The required certificate(s) referencing this Basic UDI-DI have not been registered yet.

Critical warnings

1 warning recorded — scroll inside the panel to see all entries.

CW999
Read the instructions for use and warnings before using the product. Do not use on or around eyes, burns, areas with infection, or inside wounds. Contains cyanoacrylate. Danger. It adheres to the skin and eyes in a few seconds. Keep out of reach of children. In case of contact with eyes, rinse with plenty of water for several minutes. Remove contact lenses if you wear it and it is easy. Keep rinsing.

Market distribution

Primary placement in Spain; available across 1 country total.

Placed on the market in Spain; per-country availability dates not published.

Device identification

Trade name: DERM·X
UDI-DI code: 08437016047194
Basic UDI-DI: 84370CUME154ED
Reference / catalog number: CU-ME-154-1
Issuing entity: GS1

Classification

Risk category: Class I
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: Skin Protectant. Applied in a very thin layer, solidifies in seconds forming a protective layer that acts as mechanical barrier and minimise the risk of infection. Slougs off naturally as healing occurs.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

M03030202SKIN PROTECTIVE BANDAGES

Compliance flags

Safety

Sterile

Single use

Contains latex

Reprocessed single-use

Direct marking

Substances

CMR substance

Endocrine disruptor

Regulatory

Annex XVI applicable

Sterilization

Lifecycle

New device

UDI-PI traceability

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