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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 Posture Corrector — 12 UDI-DI variants, MDR (SANKOM SA)

MD Atlas
SANKOM SA

Data from EUDAMED, last updated May 23, 2026

SANKOM Posture Corrector

7640125931210010177

12 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: 7640125931210010177
Device name: SANKOM Posture Corrector
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Mar 25, 2026

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

12 UDI-DI variants

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Applied filters

basicUdiUlid01KMH3E8K31BR4N2JG5F8RR3K9

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

SANKOM07640125931396
SANKOM07640125931341
SANKOM07640125931334
SANKOM07640125931419
SANKOM07640125931402
SANKOM07640125931365
SANKOM07640125931372
SANKOM07640125931327
SANKOM07640125931310
SANKOM07640125931389
SANKOM07640125931303
SANKOM07640125931426