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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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ARCOS DE MOVIMIENTO — 9 UDI-DI variants, MDR (ORTOTECSA,S.L.)

MD Atlas
ORTOTECSA,S.L.

Data from EUDAMED, last updated May 23, 2026

ARCOS DE MOVIMIENTO

843660217AMUR

9 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: 843660217AMUR
Device name: ARCOS DE MOVIMIENTO
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

9 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KR125TF3Z5KT35R04CDAM3PP

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.42/5008436602171787
F.40/4208436602171626
F.40/41-1/108436602179622
F.42/4808436602171756
F.40/41-408436602171619
F.40/4108436602178113
F.40/41-208436602171596
F.40/40-1/108436602171572
F.40/40-108436602171565