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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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BIOXAL M — 2 UDI-DI variants, MDR (BIOXAL)

MD Atlas
BIOXAL

Data from EUDAMED, last updated May 19, 2026

BIOXAL M

426070938BIOXAL-BUDI-01M3

2 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class IIb

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Manufacturer: BIOXAL

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 426070938BIOXAL-BUDI-01M3
Device name: BIOXAL M
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: Apr 29, 2026

Manufacturer & authorised representative

Manufacturer

Name: BIOXAL
SRN: FR-MF-000000481
Country: France
Email: alicia.deprez@schuelke.com
Phone: +33 3 85 92 30 35

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01KQBW5HAAJ8YZ44SQQNRM325T

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

7000404804260709380438
7000404704260709380414