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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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ARDYS-PLUS — 49 UDI-DI variants, MDR (NORMAGRUP TECHNOLOGY, S.A.)

MD Atlas
NORMAGRUP TECHNOLOGY, S.A.

Data from EUDAMED, last updated May 23, 2026

ARDYS-PLUS

84354041ARDYS-PLUSYF

49 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Manufacturer: NORMAGRUP TECHNOLOGY, S.A.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 84354041ARDYS-PLUSYF
Device name: ARDYS-PLUS
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: Dec 18, 2024

Manufacturer & authorised representative

Manufacturer

Name: NORMAGRUP TECHNOLOGY, S.A.
SRN: ES-MF-000013355
Country: Spain
Email: eudamed@normagrup.com
Phone: +34985267100

Variants by status

UDI-DI variants

49 UDI-DI variants

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Applied filters

basicUdiUlid01JFCHVKC5VG7F8Y4TYGYABX0H

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

No registered UDI-DI variants for this device family.