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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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SANKOM CLASSIC Socks — 6 UDI-DI variants, MDR (SANKOM SA)

MD Atlas
SANKOM SA

Data from EUDAMED, last updated May 23, 2026

SANKOM CLASSIC Socks

7640125930450111AP

6 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class I

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: SANKOM SA

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 7640125930450111AP
Device name: SANKOM CLASSIC Socks
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 25, 2025

Manufacturer & authorised representative

Manufacturer

Name: SANKOM SA
SRN: CH-MF-000047525
Country: Switzerland
Email: info@sankom.com
Phone: +41324225000

Authorised representative

Name: Roberto Sanchez Beltran
SRN: ES-AR-000047367
Country: Spain
Phone: +34635357766

Variants by status

UDI-DI variants

6 UDI-DI variants

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basicUdiUlid01JSMY20668CM0M4259RG45RVT

Format

Summary

29 columns included

Trade name
Basic UDI-DI
UDI-DI code
Risk category
Applicable legislation
Status
Organization name
SRN
Reference / catalog number
Additional product description
Intended medical purpose
Placed on the market (country)
Market info update date
Sterile
Single use
Contains latex
Reprocessed single-use
Direct marking
CMR substance
Endocrine disruptor
Annex XVI applicable
Sterilization
OEM applicable
EMDN codes
Last updated
Basic UDI-DI device name
Basic UDI-DI device model
Basic UDI-DI implantable
Basic UDI-DI reagent

SAN-045CBL Black Plus II07640125937688
SAN-045CGR Grey Plus I07640125937640
SAN-045CBL Black Plus III07640125937695
SAN-045CGR Grey Plus II07640125937657
SAN-045CGR Grey Plus III07640125937664
SAN-045CBL Black Plus I07640125937671