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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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Supramid Aragó — 59 UDI-DI variants, MDR (Laboratorio Aragó S.L.)

MD Atlas
Laboratorio Aragó S.L.

Data from EUDAMED, last updated May 23, 2026

Supramid Aragó

8427599DTTF0247F

59 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class IIb

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Manufacturer: Laboratorio Aragó S.L.

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Device characteristics

Implantable

Identity & classification

Basic UDI-DI: 8427599DTTF0247F
Device name: Supramid Aragó
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: May 7, 2026

Manufacturer & authorised representative

Manufacturer

Name: Laboratorio Aragó S.L.
SRN: ES-MF-000001958
Country: Spain
Email: eudamed@laboratorioarago.com

Variants by status

UDI-DI variants

59 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KR18EFC8JHS359NMQJV2E1MH

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

Supramid Aragó08427599023517
Supramid Aragó08427599023876
Supramid Aragó08427599023678
Supramid Aragó08427599023739
Supramid Aragó08427599025870
Supramid Aragó08427599023654
Supramid Aragó08427599023616
Supramid Aragó08427599023609
Supramid Aragó08427599023920

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