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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

AXINON® serum kit 2.0 for 100 tests — IVDD — General IVDD

MD Atlas
numares AG

EUDAMED last updated this device on May 11, 2026

AXINON® serum kit 2.0 for 100 tests

B-04260539610255

On the marketIVDD — General

Applicable legislation: IVDD [Directive 98/79/EC on in vitro diagnostic medical devices]
Organization name: numares AG
UDI-DI code: 04260539610255
Reference / catalog number: AX0315-100

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Manufacturer information

Organization name: numares AG
SRN: DE-MF-000022282
Manufacturer status: Active

Market distribution

Primary placement in Germany; available across 1 country total.

Country	On market since	Until
GermanyPrimary placement		Still on market

Device identification

Trade name: AXINON® serum kit 2.0 for 100 tests
UDI-DI code: 04260539610255
Basic UDI-DI: B-04260539610255
Reference / catalog number: AX0315-100
Issuing entity: GS1

Classification

Risk category: IVDD — General
Applicable legislation: IVDD [Directive 98/79/EC on in vitro diagnostic medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: The AXINON ® serum kit 2.0 is intended for the preparation of standardized samples from human serum for the analysis by NMR (nuclear magnetic resonance) spectroscopy in a clinical or research laboratory. In addition, it enables the calibration and quality control of NMR spectroscopic analyses by the AXINON ® System. For professional use only.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

W01010499MULTIPLE CLIN. CHEM LAB REAGENTS - OTHER

Compliance flags

Safety

Sterile

Single use

Direct marking

Regulatory

Sterilization

Lifecycle

New device

UDI-PI traceability

Batch number
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Manufacturing date
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Software identification

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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.