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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 1500 lumbar spine orthosis… — 8 UDI-DI variants, MDR

MD Atlas
ARIES, a.s.

Data from EUDAMED, last updated May 23, 2026

BrownGuard 1500 lumbar spine orthosis type 02

85900722026173S

8 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: 85900722026173S
Device name: BrownGuard 1500 lumbar spine orthosis type 02
Device model: Lumbar spine orthosis
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 21, 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

8 UDI-DI variants

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Applied filters

basicUdiUlid01KS5Z7XMJFMF5DADEEFXWKWTV

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

NA08590072970001
NA08590072969968
NA08590072969951
NA08590072969975
NA08590072969944
NA08590072969982
NA08590072969999
NA08590072970018