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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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TRACCIÓN — 12 UDI-DI variants, MDR (ORTOTECSA,S.L.)

MD Atlas
ORTOTECSA,S.L.

Data from EUDAMED, last updated May 23, 2026

TRACCIÓN

843660217TRWU

12 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: ORTOTECSA,S.L.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 843660217TRWU
Device name: TRACCIÓN
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 7, 2026

Manufacturer & authorised representative

Manufacturer

Name: ORTOTECSA,S.L.
SRN: ES-MF-000004786
Country: Spain
Email: info@ortotecsa.com
Phone: +34918719132

Variants by status

UDI-DI variants

12 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KR1G6J74QT2JJTC7E1R8B7DS

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

F.7908436602172296
F.25/608436602171091
F.25/408436602171084
F.42/2008436602171701
F.2608436602171107
F.42/4208436602171718
F.42/4308436602171725
F.42/43-3608436602178038
F.42/43-C08436602178717
F.2508436602171039
F.25/108436602171053
F.14-1N08436602170728