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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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ORTESIS NEOPRENO — 10 UDI-DI variants, MDR (EUROPODEX S.L.)

MD Atlas
EUROPODEX S.L.

Data from EUDAMED, last updated May 31, 2026

ORTESIS NEOPRENO

84370088420024N

10 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: EUROPODEX S.L.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 84370088420024N
Device name: ORTESIS NEOPRENO
Device model: E4100,E4200,E4300,E4400,E4500,E4600,E4700,E4800
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 27, 2026

Manufacturer & authorised representative

Manufacturer

Name: EUROPODEX S.L.
SRN: ES-MF-000042401
Country: Spain
Email: info@europodex.com
Phone: +34 9 8599 08 33

Variants by status

UDI-DI variants

10 UDI-DI variants

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Applied filters

basicUdiUlid01KSJKWJMJD6RSS2A2Q0V2EFNM

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

E470008437008842110
E430008437008842073
E410008437008842059
E420008437008842066
E460008437008842103
E1000A08437008842851
E100008437026339333
E440008437008842080
E450008437008842097
E480008437008842127