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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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TLSO RECTUS — 13 UDI-DI variants, MDR (Ortoiberica S.L.)

MD Atlas
Ortoiberica S.L.

Data from EUDAMED, last updated May 23, 2026

TLSO RECTUS

84311841740000NN

13 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: 84311841740000NN
Device name: TLSO RECTUS
Device model: X-1740-000
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

13 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01HEW8GMY20A8CS08HDKZESCSS

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-1740-00008431184174003
X-1742-00108431184174218
X-1742-00408431184174249
X-1742-00308431184174232
X-1742-00208431184174225
X-1742-00508431184174256
X-1742-00608431184174263
X-1741-00408431184174140
X-1741-00308431184174133
X-1741-00208431184174126
X-1741-00508431184174157
X-1741-00108431184174119
X-1741-00608431184174164