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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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BiodDil MN5 — 2 UDI-DI variants, IVDR (Bioxol Kft)

MD Atlas
Bioxol Kft

Data from EUDAMED, last updated May 24, 2026

BiodDil MN5

5999862366BioDilMN5XG

2 UDI-DI variants

IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]IVDR Class A

Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Manufacturer: Bioxol Kft

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Device characteristics

ReagentProfessional testing

Identity & classification

Basic UDI-DI: 5999862366BioDilMN5XG
Device name: —
Device model: BiodDil MN5
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Version date: Feb 3, 2023

Manufacturer & authorised representative

Manufacturer

Name: Bioxol Kft
SRN: HU-MF-000025409
Country: Hungary
Email: hemat@bioxol.com

Variants by status

UDI-DI variants

2 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01GRB4NFNS7YF9HHCZ1WJ3RJRF

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

BioDil MN5 diluent 10L05999862366186
BioDil MN5 diluent 20L05999862366193