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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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ORTEX 032 Ortéza ramenní — 5 UDI-DI variants, MDR

MD Atlas
ORTEX , spol. s r.o.

Data from EUDAMED, last updated Jun 2, 2026

ORTEX 032 Ortéza ramenní

85955714ORTEX032ND

5 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: ORTEX , spol. s r.o.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 85955714ORTEX032ND
Device name: ORTEX 032 Ortéza ramenní
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 31, 2026

Manufacturer & authorised representative

Manufacturer

Name: ORTEX , spol. s r.o.
SRN: CZ-MF-000048500
Country: Czechia
Email: ortexzlin@ortexzlin.cz
Phone: +420577011272

Variants by status

UDI-DI variants

5 UDI-DI variants

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Applied filters

basicUdiUlid01KSZ0AYZ8D8YVZGQA77M36FQV

Format

Summary

30 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
Market country
Issuing entity
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

ORTEX 032 Shoulder brace08595571404613
ORTEX 032 Shoulder brace08595571404606
ORTEX 032 Shoulder brace08595571404620
ORTEX 032 Shoulder brace08595571404590
ORTEX 032 Shoulder brace08595571404583