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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

My Day Lady MINI — Class I MDR by CMC Consumer Medical…

MD Atlas
CMC Consumer Medical Care GmbH

EUDAMED last updated this device on May 7, 2026

My Day Lady MINI

40424413709HK

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: CMC Consumer Medical Care GmbH
UDI-DI code: 04046871004088
Reference / catalog number: 180001

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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
Do not flush down the toilet.
CW999
Keep plastic bags away from babies and children to avoid suffocation.
CW009
EUDAMED did not publish a description for this code.

Market distribution

Primary placement in France; available across 3 countries total.

Country	On market since	Until
FrancePrimary placement		Still on market
Belgium		Still on market
Spain		Still on market

Device identification

Trade name: My Day Lady MINI
UDI-DI code: 04046871004088
Basic UDI-DI: 40424413709HK
Reference / catalog number: 180001
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: 16
Additional product description: —
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: MINI

EMDN nomenclature code(s)

T04010102SHAPED INCONTINENCE NAPPIES

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