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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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Pulsed Magnetic Therapy Device BIOMAG® — 4 UDI-DI variants, MDR

MD Atlas
Karel Hrnčíř - BIOMAG

Data from EUDAMED, last updated May 23, 2026

Pulsed Magnetic Therapy Device BIOMAG®

859420828BIOMAGLUMINA3DSA

4 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: Karel Hrnčíř - BIOMAG

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Device characteristics

Active device

Clinical investigations

Registered: No

Identity & classification

Basic UDI-DI: 859420828BIOMAGLUMINA3DSA
Device name: Pulsed Magnetic Therapy Device BIOMAG®
Device model: BIOMAG® Lumina 3D-e s aplikátory
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: May 18, 2026

Manufacturer & authorised representative

Manufacturer

Name: Karel Hrnčíř - BIOMAG
SRN: CZ-MF-000025009
Country: Czechia
Email: biomag@biomag.cz
Phone: +420 493691730

Variants by status

UDI-DI variants

4 UDI-DI variants

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Applied filters

basicUdiUlid01KRXRZMNRSVMFWXMEFKTRQ2DC

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

LUMINA 3D-e EA08594208280019
LUMINA 3D-e CA08594208280033
LUMINA 3D-e EB08594208280026
LUMINA 3D-e CB08594208280040