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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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ENFORCE Active Foot — 4 UDI-DI variants, MDR

MD Atlas
ENforce Medical Technologies Sp. z o.o.

Data from EUDAMED, last updated May 30, 2026

ENFORCE Active Foot

59054969507ACTIVEFOOT75

4 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: ENforce Medical Technologies Sp. z o.o.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 59054969507ACTIVEFOOT75
Device name: ENFORCE Active Foot
Device model: EAF13,EAF14,EAF15,EAF33,EAF34,EAF35,EAF53,EAF54,EAF55,EAF63,EAF64,EAF65
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Feb 14, 2025

Manufacturer & authorised representative

Manufacturer

Name: ENforce Medical Technologies Sp. z o.o.
SRN: PL-MF-000043797
Country: Poland
Email: biuro@enforcemed.pl

Variants by status

UDI-DI variants

4 UDI-DI variants

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Applied filters

basicUdiUlid01JM1W9EV6AHXX415JKNVMX8SF

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

ENFORCE Active Foot05906952972189
ENFORCE Active Foot05906952972196
ENFORCE Active Foot05906952972202
ENFORCE Active Foot05906952972219