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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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FOOTLOGICS HIGH HEEL XS — 6 UDI-DI variants, MDR

MD Atlas
Footlogics Europe B.V.

Data from EUDAMED, last updated May 30, 2026

FOOTLOGICS HIGH HEEL XS

8721161974FTLSHIGHHEELTN

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: Footlogics Europe B.V.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 8721161974FTLSHIGHHEELTN
Device name: FOOTLOGICS HIGH HEEL XS
Device model: FOOTLOGICS HIGH HEEL
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 30, 2025

Manufacturer & authorised representative

Manufacturer

Name: Footlogics Europe B.V.
SRN: NL-MF-000043504
Country: Netherlands
Email: info@footlogics.nl
Phone: +31 036 5260 888

Variants by status

UDI-DI variants

6 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01JWGGMGC6WNNWWVPRXFQQS75Q

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

FOOTLOGICS HIGH HEEL INSOLE M08721161974055
FOOTLOGICS HIGH HEEL INSOLE M08721161974116
FOOTLOGICS HIGH HEEL INSOLE S08721161974529
FOOTLOGICS HIGH HEEL INSOLE S08721161974321
FOOTLOGICS HIGH HEEL INSOLE XS08721161974314
FOOTLOGICS HIGH HEEL INSOLE XS08721161974512