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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

SOCQUETTE PROTECTION TALON — Class I MDR by MCCB

MD Atlas
MCCB

EUDAMED last updated this device on May 19, 2026

SOCQUETTE PROTECTION TALON

37007277TALVL

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: MCCB
UDI-DI code: 03700727700227
Reference / catalog number: ITWS

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Manufacturer information

Organization name: MCCB
SRN: FR-MF-000033217
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

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

CW011
Dot not use directly on skin lesions (wound)
CW010
EUDAMED did not publish a description for this code.

Market distribution

Primary placement in France; available across 1 country total.

Country	On market since	Until
FrancePrimary placement		Still on market

Device identification

Trade name: SOCQUETTE PROTECTION TALON
UDI-DI code: 03700727700227
Basic UDI-DI: 37007277TALVL
Reference / catalog number: ITWS
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: Socquette talons secs, crevassés blanche en 35-38
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: 35–38 MU161

EMDN nomenclature code(s)

Y0999PERSONAL CARE AIDS - 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

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
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Software identification