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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 — 6 UDI-DI variants, MDR (NORMAGRUP TECHNOLOGY, S.A.)

MD Atlas
NORMAGRUP TECHNOLOGY, S.A.

Data from EUDAMED, last updated May 23, 2026

ARDYS

84354041ARDYSLD

6 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

Administers medicine

Identity & classification

Basic UDI-DI: 84354041ARDYSLD
Device name: ARDYS
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

6 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01JC04WWVZSC6DP37P70NEBK1K

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

Ardys-PD08435404196615
Ardys-DS08435404198923
Ardys-D08435404199647
Ardys08435404199722
Ardys-S08435404196349
Ardys-P08435404197148