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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

220973.2 — Class I MDR by Laboratorios Cinfa, S.A.

MD Atlas
Laboratorios Cinfa, S.A.

EUDAMED last updated this device on Jan 29, 2026

220973.2

8430469calcetinelastico34

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Laboratorios Cinfa, S.A.
UDI-DI code: 08430469236603
Reference / catalog number: 220973.2

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Manufacturer information

Organization name: Laboratorios Cinfa, S.A.
SRN: ES-MF-000001574
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

1 warning recorded — scroll inside the panel to see all entries.

CW010
No utilizar en caso de enfermedad obstructiva arterial periférica en estado avanzado, insuficiencia cardiaca descompensada, flebitis séptica, flegmasia cerúlea dolens, presentar alergia a los materiales de la prenda, neuropatía periférica en estado avanzado por diabetes melitus

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: 08430469236603
Basic UDI-DI: 8430469calcetinelastico34
Reference / catalog number: 220973.2
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: No clinical sizes registered for this device.

EMDN nomenclature code(s)

M030405COMPRESSION STOCKINGS

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
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Software identification