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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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INMOVILIZADOR RODILLA — 5 UDI-DI variants, MDR (Junquera y Diz S.L.)

MD Atlas
Junquera y Diz S.L.

Data from EUDAMED, last updated May 23, 2026

INMOVILIZADOR RODILLA

843567120112EJ

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: Junquera y Diz S.L.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 843567120112EJ
Device name: INMOVILIZADOR RODILLA
Device model: INMOVILIZADOR DE RODILLA
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Mar 22, 2022

Manufacturer & authorised representative

Manufacturer

Name: Junquera y Diz S.L.
SRN: ES-MF-000002269
Country: Spain
Email: info@junqueraydiz.es
Phone: +34 985161666

Variants by status

UDI-DI variants

5 UDI-DI variants

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Applied filters

basicUdiUlid01FTME5HFY20PCTWX41Z1AK0MB

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

RII-001-700008435671260668
RII-001-500008435671260644
RII-001-600008435671260651
RII-001-400008435671260637
RII-00208435671265205