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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 SENSI INSOLE — 9 UDI-DI variants, MDR

MD Atlas
Footlogics Europe B.V.

Data from EUDAMED, last updated May 30, 2026

FOOTLOGICS SENSI INSOLE

8721161974FTLSSENSI6A

9 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: 8721161974FTLSSENSI6A
Device name: FOOTLOGICS SENSI INSOLE
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 22, 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

9 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01JVVKZ03ZCQFND49D5N25CZRB

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

FOOTLOGIC SENSI INSOLE XS08721161974284
FOOTLOGICS SENSI INSOLE L08721161974048
FOOTLOGICS SENSI INSOLE L08721161974109
FOOTLOGICS SENSI INSOLE M08721161974505
FOOTLOGICS SENSI INSOLE M08721161974307
FOOTLOGICS SENSI INSOLE S08721161974499
FOOTLOGICS SENSI INSOLE XL08721161974567
FOOTLOGICS SENSI INSOLE XL08721161974550
FOOTLOGICS SENSI INSOLE XS08721161974482