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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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ALGODÓN HIDRÓFILO 100% PURO — 2 UDI-DI variants, MDR

MD Atlas
Laboratorios Indas, S.A.U

Data from EUDAMED, last updated May 23, 2026

ALGODÓN HIDRÓFILO 100% PURO

8410520AZZCY

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 Indas, S.A.U

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 8410520AZZCY
Device name: ALGODÓN HIDRÓFILO 100% PURO
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Dec 14, 2021

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

2 UDI-DI variants

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Applied filters

basicUdiUlid01FPWN6H9P783Z3ZV4P4EZJYKW

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

340300408410520014944
340300308410520030036