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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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FERULA STACK DISTAL — 10 UDI-DI variants, MDR (Ortoiberica S.L.)

MD Atlas
Ortoiberica S.L.

Data from EUDAMED, last updated May 23, 2026

FERULA STACK DISTAL

8431184X5010PY

10 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: 8431184X5010PY
Device name: FERULA STACK DISTAL
Device model: X-5010-
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Feb 27, 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

10 UDI-DI variants

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Applied filters

basicUdiUlid01HQN4CYEVRQ3XPKNN3W93GXJV

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

X-5010-08431184501007
X-5010-00108431184501014
X-5010-00208431184501021
X-5010-00308431184501038
X-5010-00408431184501045
X-5010-00508431184501052
X-5010-05508431184501557
X-5010-00608431184501069
X-5010-00708431184501076
X-5010-00008431184954100