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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

CUME013-1PT — Class I MDR by Cuantum Medical…

MD Atlas
Cuantum Medical Cosmetics SL

EUDAMED last updated this device on Jul 11, 2025

CUME013-1PT

84370CUME013-18N

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Cuantum Medical Cosmetics SL
UDI-DI code: 08412122180027
Reference / catalog number: CUME013-1PT

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Manufacturer information

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

Critical warnings

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

CW999
Contém cianoacrilato. Manuseie com cuidado. Perigo: Não use sobre ou ao redor dos olhos, queimaduras, áreas infectadas ou dentro de feridas. Consulte um médico para uso em casos de feridas graves e mordidas de animais. Adere à pele e aos olhos em segundos. Não use em pessoas com alergia a cianoacrilato.

Market distribution

Primary placement in Portugal; available across 1 country total.

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

Device identification

Trade name: not provided
UDI-DI code: 08412122180027
Basic UDI-DI: 84370CUME013-18N
Reference / catalog number: CUME013-1PT
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: Curativo líquido para uso tópico para proteger a pele saudável ou danificada.
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

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

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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.