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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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Boots - Everyday — 4 UDI-DI variants, MDR (Barcelcom Têxteis S.A.)

MD Atlas
Barcelcom Têxteis S.A.

Data from EUDAMED, last updated May 30, 2026

Boots - Everyday

056025416403BTJA

4 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: Barcelcom Têxteis S.A.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 056025416403BTJA
Device name: Boots - Everyday
Device model: Boots - Everyday
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Feb 4, 2025

Manufacturer & authorised representative

Manufacturer

Name: Barcelcom Têxteis S.A.
SRN: PT-MF-000036996
Country: Portugal
Email: info@barcelcomtexteis.com
Phone: +351 253849020

Variants by status

UDI-DI variants

4 UDI-DI variants

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Applied filters

basicUdiUlid01JK80JB9RY3JQ0DBBKVKGYH4X

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

Boots - Everyday05045099076562
Boots - Everyday05045099076586
Boots - Everyday05045099076579
Boots - Everyday05045099076555