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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

533270 — Class I MDR by CMC Consumer Medical…

MD Atlas
CMC Consumer Medical Care GmbH

EUDAMED last updated this device on May 7, 2026

533270

40424413715HE

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: CMC Consumer Medical Care GmbH
UDI-DI code: 04042441022858
Reference / catalog number: 533270

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Manufacturer information

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

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Critical warnings

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

CW999
Do not use in case of sensitivity to acrylic adhesive.
CW999
Ensure that the affected area is clean, dry and oil free before applying the tape.
CW009
EUDAMED did not publish a description for this code.

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: 04042441022858
Basic UDI-DI: 40424413715HE
Reference / catalog number: 533270
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: —
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: 2.5 MU10
5 MU36

EMDN nomenclature code(s)

M050101PLASTERS ON SPOOLS (ROLLS)

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

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.