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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

183451 — Class I MDR by CMC Consumer Medical…

MD Atlas
CMC Consumer Medical Care GmbH

EUDAMED last updated this device on May 7, 2026

183451

40424413707HF

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: CMC Consumer Medical Care GmbH
UDI-DI code: 04042441024326
Reference / catalog number: 183451

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Manufacturer information

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

Critical warnings

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

CW009
EUDAMED did not publish a description for this code.
CW999
Do not use on open wounds.
CW999
To avoid danger of suffocation, keep this plastic bag away from babies and children.
CW999
Change daily
CW999
Keep away from naked flames.

Market distribution

Primary placement in Spain; available across 1 country total.

Country	On market since	Until
SpainPrimary placement		Still on market

Device identification

Trade name: not provided
UDI-DI code: 04042441024326
Basic UDI-DI: 40424413707HF
Reference / catalog number: 183451
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: 100 MU24

EMDN nomenclature code(s)

M010101HYDROPHILIC COTTON

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.