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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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ROTACIÓN — 8 UDI-DI variants, MDR (ORTOTECSA,S.L.)

MD Atlas
ORTOTECSA,S.L.

Data from EUDAMED, last updated May 23, 2026

ROTACIÓN

843660217ROWG

8 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: 843660217ROWG
Device name: ROTACIÓN
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

8 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KR18XM3MRSWQS8K6P8ZBHRYQ

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.42/4908436602171770
G.617608436602174207
F.42/4608436602178076
F.42/4708436602171732
F.42/47-S08436602171749
F.42/4408436602178052
G.616008436602174184
F.22/3E08436602170919