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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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SOPORTE LUMBAR RECTUS — 7 UDI-DI variants, MDR (Ortoiberica S.L.)

MD Atlas
Ortoiberica S.L.

Data from EUDAMED, last updated May 23, 2026

SOPORTE LUMBAR RECTUS

84311841240000LM

7 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: 84311841240000LM
Device name: SOPORTE LUMBAR RECTUS
Device model: X-1240-000
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jan 7, 2026

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

7 UDI-DI variants

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Applied filters

basicUdiUlid01HEWCK9JEYJ9STQ4NQ8CZCB2T

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-1240-00008431184124008
X-1242-00308431184124237
X-1242-00208431184124220
X-1242-00108431184124213
X-1241-00308431184124138
X-1241-00208431184124121
X-1241-00108431184124114