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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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AMANHECER — 3 UDI-DI variants, MDR (Laboratorios Indas, S.A.U)

MD Atlas
Laboratorios Indas, S.A.U

Data from EUDAMED, last updated May 23, 2026

AMANHECER

5601227AALFU8

3 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 Indas, S.A.U

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 5601227AALFU8
Device name: AMANHECER
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Nov 7, 2025

Manufacturer & authorised representative

Manufacturer

Name: Laboratorios Indas, S.A.U
SRN: ES-MF-000000586
Country: Spain
Email: fabrica@indas.es
Phone: +34 915 096 000

Variants by status

UDI-DI variants

3 UDI-DI variants

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Applied filters

basicUdiUlid01K9EN3S397TTFB34Y0W19XX2B

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

387392005601227022544
387392105601227022520
387391805601227022537