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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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Compressa de celulose — 2 UDI-DI variants, MDR

MD Atlas
Albino Dias de Andrade, S.A.

Data from EUDAMED, last updated May 31, 2026

Compressa de celulose

560082989A0103WR

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: Albino Dias de Andrade, S.A.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 560082989A0103WR
Device name: Compressa de celulose
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 26, 2026

Manufacturer & authorised representative

Manufacturer

Name: Albino Dias de Andrade, S.A.
SRN: PT-MF-000002823
Country: Portugal
Email: geral@ada.pt
Phone: +351 255 890 040

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01KSJAZ7QSA8M8TNA6XK8PSP0H

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

0560084626279905600846262799
ADA Swabs05600829896928