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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

0442A5 — Class I MDR by Calzificio Pinelli Srl

MD Atlas
Calzificio Pinelli Srl

EUDAMED last updated this device on May 18, 2026

0442A5

83004960079DC23

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Calzificio Pinelli Srl
UDI-DI code: 08300496055112
Reference / catalog number: 0442A5

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View device family (Basic UDI)

Manufacturer information

Organization name: Calzificio Pinelli Srl
SRN: IT-MF-000005917
Manufacturer status: Active

Related devices

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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

No critical warnings reported for this device.

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Market distribution

Primary placement in Italy; available across 1 country total.

Country	On market since	Until
ItalyPrimary placement		Still on market

Device identification

Trade name: not provided
UDI-DI code: 08300496055112
Basic UDI-DI: 83004960079DC23
Reference / catalog number: 0442A5
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: Colour Champagne - size 1S - Ankle-sock made of the special micro-massaging fabric with threedimensional waves. This fabric activates a beneficial micro-massage on the skin and perfect skin transpiration, to keep the feet dry and at the right temperature. For everyday use and especially recommended for all types of sports activities. The anatomic compression offers a perfect foot fit.
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

UDI-DI DataMatrix

Encoded

(01)08300496055112

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UDI-PI DataMatrix

The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.

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EMDN nomenclature code(s)

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

M030499ELASTIC BANDAGES, SUPPORT AND COMPRESSION - OTHER

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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