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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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BrownGuard 5000 ankle orthosis type 01 — 6 UDI-DI variants, MDR

MD Atlas
ARIES, a.s.

Data from EUDAMED, last updated May 23, 2026

BrownGuard 5000 ankle orthosis type 01

85900722026043H

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: ARIES, a.s.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 85900722026043H
Device name: BrownGuard 5000 ankle orthosis type 01
Device model: Ankle orthosis
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 30, 2026

Manufacturer & authorised representative

Manufacturer

Name: ARIES, a.s.
SRN: CZ-MF-000047385
Country: Czechia
Email: durda@aries.eu

Variants by status

UDI-DI variants

6 UDI-DI variants

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Applied filters

basicUdiUlid01KQFVR0S2VCFYAR0X8JWF9NJ2

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

BrownGuard 5000 ankle orthosis type 0108590072961757
BrownGuard 5000 ankle orthosis type 0108590072961726
BrownGuard 5000 ankle orthosis type 0108590072961733
BrownGuard 5000 ankle orthosis type 0108590072961719
BrownGuard 5000 ankle orthosis type 0108590072961740
BrownGuard 5000 ankle orthosis type 0108590072961764