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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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ARIA — 6 UDI-DI variants, MDR (Ortoiberica S.L.)

MD Atlas
Ortoiberica S.L.

Data from EUDAMED, last updated May 23, 2026

ARIA

8431184P9017007F

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: Ortoiberica S.L.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 8431184P9017007F
Device name: ARIA
Device model: P-9014
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Mar 5, 2024

Manufacturer & authorised representative

Manufacturer

Name: Ortoiberica S.L.
SRN: ES-MF-000025780
Country: Spain
Email: welcome@ortoiberica.es
Phone: +34985794800

Variants by status

UDI-DI variants

6 UDI-DI variants

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Applied filters

basicUdiUlid01HR6Y87CBTQ4V7FQGWJWEGGSY

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

P-9014-08431184901401
P-9014-40008431184901449
P-9014-20008431184901425
P-9014-50008431184901456
P-9014-60008431184901463
P-9014-70008431184901470