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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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IMAQE Crema adhesiva 40g — 2 UDI-DI variants, MDR

MD Atlas
Laboratorios URGO S.L.

Data from EUDAMED, last updated May 23, 2026

IMAQE Crema adhesiva 40g

8413647NF310S7

2 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: 8413647NF310S7
Device name: IMAQE Crema adhesiva 40g
Device model: FÓRMULA NF-310
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Oct 30, 2025

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

2 UDI-DI variants

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Applied filters

basicUdiUlid01K8TE103ADA3ZES21RRX6N2GG

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

60496008413647049608
60307208413647030729