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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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Lifehub — 2 UDI-DI variants, MDR (BIODATA DEVICES, SL)

MD Atlas
BIODATA DEVICES, SL

Data from EUDAMED, last updated May 23, 2026

Lifehub

8437025191LIFEHUB01EM

2 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: BIODATA DEVICES, SL

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Device characteristics

Active deviceMeasuring function

Identity & classification

Basic UDI-DI: 8437025191LIFEHUB01EM
Device name: Lifehub
Device model: Lifehub
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: May 6, 2026

Manufacturer & authorised representative

Manufacturer

Name: BIODATA DEVICES, SL
SRN: ES-MF-000029454
Country: Spain
Email: regulacion@biodatadevices.es
Phone: 983704402

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01KQY5TWS1S4SP70K6Q2V8QY2A

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

00208437025191017
00108437025191000