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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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Probengefäss steril — 3 UDI-DI variants, IVDR (Axon Biotech GmbH)

MD Atlas
Axon Biotech GmbH

Data from EUDAMED, last updated May 23, 2026

Probengefäss steril

425173791166

3 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: Axon Biotech GmbH

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Device characteristics

Professional testing

Identity & classification

Basic UDI-DI: 425173791166
Device name: Probengefäss steril
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Version date: Oct 10, 2025

Manufacturer & authorised representative

Manufacturer

Name: Axon Biotech GmbH
SRN: DE-MF-000027334
Country: Germany
Email: martina.deisinger@axonbiotech.de
Phone: +49 9901 20 29 - 12

Variants by status

UDI-DI variants

3 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01K76PAMN8K9ECE6YCF0B84VQH

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

AL0513-B04251737902273
AL051304251737902266
AL051204251737902259