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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

MF325021062350 — Class I MDR by Health and Fashion…

MD Atlas
Health and Fashion Shoes Italia SpA

EUDAMED last updated this device on Apr 1, 2026

MF325021062350

805714973MEMORYCUSHIONB8

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Health and Fashion Shoes Italia SpA
UDI-DI code: 08004373631450
Reference / catalog number: MF325021062350

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View device family (Basic UDI)

Manufacturer information

Organization name: Health and Fashion Shoes Italia SpA
SRN: IT-MF-000038685
Manufacturer status: Active

Related devices

MF312901040400805714973MEMORYCUSHIONB8On the market MF312901040410805714973MEMORYCUSHIONB8On the market MF006251029470805714973MEMORYCUSHIONB8On the market MF006251029440805714973MEMORYCUSHIONB8On the market MF006251029430805714973MEMORYCUSHIONB8On the market

Critical warnings

No critical warnings reported for this device.

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Market distribution

Primary placement in Poland; available across 1 country total.

Country	On market since	Until
PolandPrimary placement		Still on market

Device identification

Trade name: not provided
UDI-DI code: 08004373631450
Basic UDI-DI: 805714973MEMORYCUSHIONB8
Reference / catalog number: MF325021062350
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: COLOR TAUPE
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

EMDN nomenclature code(s)

European Medical Device Nomenclature — the EU product classification assigned to this device.

Y061203ORTHOSES, FOOT (INCLUDING INSOLES AND INSERTS)

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

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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.