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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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ADA Swabs — 134 UDI-DI variants, MDR (Albino Dias de Andrade, S.A.)

MD Atlas
Albino Dias de Andrade, S.A.

Data from EUDAMED, last updated May 31, 2026

ADA Swabs

560082989C0103XF

134 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: Albino Dias de Andrade, S.A.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 560082989C0103XF
Device name: —
Device model: ADA Swabs
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Jun 11, 2025

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

134 UDI-DI variants

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Applied filters

basicUdiUlid01JXFR3REF8AVP85PZJ6AR6AQ4

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

ADA Swabs15600829898585
ADA Swabs15600829898844
ADA Swabs15600701940319
ADA Swabs05600846260320
ADA Swabs05600846267411
ADA Swabs15600829894020
UCGE05600846267985
UCGE05600846264557
VidWell05600846267237

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