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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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Actif — 2 UDI-DI variants, MDR (Actif Age Lda)

MD Atlas
Actif Age Lda

Data from EUDAMED, last updated May 30, 2026

Actif

56006100855ACTIFJA

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: Actif Age Lda

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Device characteristics

Active deviceMeasuring function

Identity & classification

Basic UDI-DI: 56006100855ACTIFJA
Device name: Actif
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Sep 26, 2024

Manufacturer & authorised representative

Manufacturer

Name: Actif Age Lda
SRN: PT-MF-000044037
Country: Portugal
Email: sara@actif.online
Phone: +351914056541

Variants by status

UDI-DI variants

2 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01J6SHVKWHW5PQ292WNBQDF8SS

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

Actif for Individuals05600610085517
Actif for Professionals05600610085500