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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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Bryterarm til rails — 1 UDI-DI variant, MDR (Ergo Contech)

MD Atlas
Ergo Contech

Data from EUDAMED, last updated May 30, 2026

Bryterarm til rails

90056600014LV

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: Ergo Contech

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 90056600014LV
Device name: Bryterarm til rails
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jul 29, 2022

Manufacturer & authorised representative

Manufacturer

Name: Ergo Contech
SRN: NO-MF-000002649
Country: Norway
Email: post@ergocontech.no
Phone: +47 4000 1765

Variants by status

UDI-DI variants

1 UDI-DI variant

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Applied filters

basicUdiUlid01G94BKVMSVM75VFYQF61FF192

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

1409005660000149