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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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HIDROTERAPIA — 14 UDI-DI variants, MDR (ORTOTECSA,S.L.)

MD Atlas
ORTOTECSA,S.L.

Data from EUDAMED, last updated May 23, 2026

HIDROTERAPIA

843660217HDUU

14 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: 843660217HDUU
Device name: HIDROTERAPIA
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

14 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KR1792YYSBD4F285E6PK7R29

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

G.18951/D08436602174016
G.18951/22008436602173743
G.18951/40008436602173835
G.18951/B08436602173927
G.18951/C08436602173989
G.18951/29008436602173774
G.18951/E08436602174047
G.18951/34008436602173804
G.18951/A08436602173866
G.1895408436602179769
G.1895308436602179745
G.1895708436602174108
G.18957-A08436602174177
G.18951/100008436602173712