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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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Faja sacrolumbar semirrígida corta — 10 UDI-DI variants, MDR

MD Atlas
Orliman, S.L.U.

Data from EUDAMED, last updated May 23, 2026

Faja sacrolumbar semirrígida corta

84350259ORL20201PC

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: Orliman, S.L.U.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 84350259ORL20201PC
Device name: Faja sacrolumbar semirrígida corta
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jan 25, 2022

Manufacturer & authorised representative

Manufacturer

Name: Orliman, S.L.U.
SRN: ES-MF-000001598
Country: Spain
Email: eudamed@orliman.es
Phone: +34 962725704

Variants by status

UDI-DI variants

10 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01FT8VBD9MHPTFBC78ZJ84N9XE

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

EV-100#N108435025954168
EV-100#N208435025954175
EV-100#N708435025954229
EV-100#N1008435025997950
EV-100#N308435025954182
EV-100#N908435025991187
EV-100#N608435025954212
EV-100#N408435025954199
EV-100#N808435025954236
EV-100#N508435025954205