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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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Bmotion Foldable Walker AN200 — 1 UDI-DI variant, MDR

MD Atlas
Evoluxion Health, Lda

Data from EUDAMED, last updated May 30, 2026

Bmotion Foldable Walker AN200

5600728191AN200PF

1 UDI-DI variant

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: Evoluxion Health, Lda

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 5600728191AN200PF
Device name: Bmotion Foldable Walker AN200
Device model: Bmotion Foldable Walker AN200
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 24, 2026

Manufacturer & authorised representative

Manufacturer

Name: Evoluxion Health, Lda
SRN: PT-MF-000043932
Country: Portugal
Email: export@evoluxionhealth.com
Phone: +351 925 568 105

Variants by status

UDI-DI variants

1 UDI-DI variant

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Applied filters

basicUdiUlid01KP5JZFTGRAZTJMEM0QVZPC1F

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

Bmotion Foldable Walker05600728191841