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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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MOBILIARIO ESPECIAL ADAPTADO — 16 UDI-DI variants, MDR

MD Atlas
ORTOTECSA,S.L.

Data from EUDAMED, last updated May 23, 2026

MOBILIARIO ESPECIAL ADAPTADO

843660217MOVZ

16 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: 843660217MOVZ
Device name: MOBILIARIO ESPECIAL ADAPTADO
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

16 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KR17N0YC2VGY3QXDAAF7TR0S

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

T.P.100408436602174993
T.P.1712-C08436602175938
T.P.1712-B08436602175884
T.P.1712-A08436602175839
T.P.100608436602175006
T.P.1006/B08436602175013
T.P.1006/C08436602175037
T.P.1000/G-E08436602174979
T.P.1000-E08436602174986
T.P.1000/G08436602174962
T.P.1100/208436602175143
T.P.1100/108436602175075
T.P.110008436602175068
T.P.115608436602175273
T.P.125008436602175563
T.P.100008436602174955