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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

8480480 — Class I MDR by CMC Consumer Medical…

MD Atlas
CMC Consumer Medical Care GmbH

EUDAMED last updated this device on May 7, 2026

8480480

40424413712H8

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: CMC Consumer Medical Care GmbH
UDI-DI code: 04042441014013
Reference / catalog number: 8480480

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Manufacturer information

Organization name: CMC Consumer Medical Care GmbH
SRN: DE-MF-000006178
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

3 warnings recorded — scroll inside the panel to see all entries.

CW999
Ensure that the affected area is clean, dry and oil free before applying the plaster
CW009
EUDAMED did not publish a description for this code.
CW999
Change plaster at least once a day

Market distribution

Primary placement in Germany; available across 1 country total.

Country	On market since	Until
GermanyPrimary placement		Still on market

Device identification

Trade name: not provided
UDI-DI code: 04042441014013
Basic UDI-DI: 40424413712H8
Reference / catalog number: 8480480
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: 20
Additional product description: —
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: 100 MU50
60 MU50

EMDN nomenclature code(s)

M04010102POLYURETHANE (OR OTHER MATERIAL) ADHESIVE DRESSINGS, WITH ABSORBENT PAD

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