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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

SAN-045CBL Black Plus III — Class I MDR by SANKOM SA

MD Atlas
SANKOM SA

EUDAMED last updated this device on Apr 25, 2025

SAN-045CBL Black Plus III

7640125930450111AP

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: SANKOM SA
UDI-DI code: 07640125937695
Reference / catalog number: SAN-045CBL Black Plus III

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Manufacturer information

Organization name: SANKOM SA
SRN: CH-MF-000047525
Manufacturer status: Active

Market distribution

Primary placement in Spain; available across 1 country total.

Placed on the market in Spain; per-country availability dates not published.

Device identification

Trade name: not provided
UDI-DI code: 07640125937695
Basic UDI-DI: 7640125930450111AP
Reference / catalog number: SAN-045CBL Black Plus III
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: Intended Purpose: The SANKOM Patent Socks are clinically proven to combat vascular conditions such as Deep Vein Thrombosis and Varicose Veins. They use active graduated targeted compression to help evacuate venous blood from the legs and improve blood circulation, increasing circulation efficiency and reducing discomfort, pain and heaviness due to circulation problems. Prevents swelling, pain, edema and Deep Vein Thrombosis or reduces their symptoms.
Additional information URL: https://www.sankom.com/pages/socks
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
Serial number
Software identification

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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.