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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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AL0202 — 12 UDI-DI variants, IVDR (Axon Biotech GmbH)

MD Atlas
Axon Biotech GmbH

Data from EUDAMED, last updated May 23, 2026

AL0202

425173790265

12 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: 425173790265
Device name: —
Device model: AL0202
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Version date: Aug 27, 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

12 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01K3NGFZWRG09D9WG0PQ1YAWPW

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

AL020204251737900019
AL0202DL04251737900057
AL0205DL04251737900170
AL020504251737900156
AL020304251737900118
AL0203DL04251737900132
AL020604251737900194
AL0206DL04251737900217
AL020104251737900095
0813660204251737902204
0813660304251737902211
102245004251737902495