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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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NOVAFIX PRO3 FRESCOR 20 G — 5 UDI-DI variants, MDR

MD Atlas
Laboratorios URGO S.L.

Data from EUDAMED, last updated May 23, 2026

NOVAFIX PRO3 FRESCOR 20 G

8413647ULTRAFUERTEL8

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: Laboratorios URGO S.L.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 8413647ULTRAFUERTEL8
Device name: NOVAFIX PRO3 FRESCOR 20 G
Device model: FÓRMULA ULTRAFUERTE
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Oct 26, 2022

Manufacturer & authorised representative

Manufacturer

Name: Laboratorios URGO S.L.
SRN: ES-MF-000000629
Country: Spain
Email: administracion@es.urgo.com
Phone: +34 943 33 50 57

Variants by status

UDI-DI variants

5 UDI-DI variants

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Applied filters

basicUdiUlid01G5RCYS4DQE7AFBTGD0EFBB59

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

60423908413647042395
ES000526008413647052608
ES000526108413647052615
ES000529008413647052905
ES000505108413647050512