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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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Organization name
UDI-DI code
Reference / catalog number

AL0206DL — IVDR Class A IVDR by Axon Biotech GmbH

MD Atlas
Axon Biotech GmbH

EUDAMED last updated this device on Aug 27, 2025

AL0206DL

425173790265

On the marketIVDR Class A

Applicable legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Organization name: Axon Biotech GmbH
UDI-DI code: 04251737900217
Reference / catalog number: AL0206DL

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Manufacturer information

Organization name: Axon Biotech GmbH
SRN: DE-MF-000027334
Manufacturer status: Active

Related devices

AL0135425173790163On the market 51010142517379096KOn the market AL060242517379066DOn the market AL0310425173790367On the market 51053642517379096KOn the market

Certificates

No certificates registered for this manufacturer.

No certificate references this Basic UDI-DI, because: • It does not require a certificate, or • It only requires a certificate without a Basic UDI-DI reference (e.g. a QMS certificate), or • The required certificate(s) referencing this Basic UDI-DI have not been registered yet.

Critical warnings

2 warnings recorded — scroll inside the panel to see all entries.

CW009
EUDAMED did not publish a description for this code.
CW007
EUDAMED did not publish a description for this code.

Market distribution

Primary placement in Germany; available across 1 country total.

Placed on the market in Germany; per-country availability dates not published.

Device identification

Trade name: not provided
UDI-DI code: 04251737900217
Basic UDI-DI: 425173790265
Reference / catalog number: AL0206DL
Issuing entity: GS1

Classification

Risk category: IVDR Class A
Applicable legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Status: On the market

Device details

Quantity: 10
Additional product description: —
Additional information URL: https://www.axonbiotech.de/category/download-center/gebrauchsanweisungen
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

W0104010703URINE SCREENING MANUAL (DIPSLIDES ETC.)

Compliance flags

Safety

Sterile

Single use

Direct marking

Regulatory

Sterilization

Lifecycle

New device

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
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Software identification