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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

Panel A320 — IVDD — General IVDD by MEDIWISS ANALYTIC GmbH…

MD Atlas
MEDIWISS ANALYTIC GmbH Gesellschaft für angewandte in-vitro Analytik

EUDAMED last updated this device on Jan 28, 2026

Panel A320

B-04251342603206

On the marketIVDD — General

Applicable legislation: IVDD [Directive 98/79/EC on in vitro diagnostic medical devices]
Organization name: MEDIWISS ANALYTIC GmbH Gesellschaft für angewandte in-vitro Analytik
UDI-DI code: 04251342603206
Reference / catalog number: 0320

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Manufacturer information

Organization name: MEDIWISS ANALYTIC GmbH Gesellschaft für angewandte in-vitro Analytik
SRN: DE-MF-000004992
Manufacturer status: Active

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Critical warnings

1 warning recorded — scroll inside the panel to see all entries.

CW010
See Instructions for use point 7. Warning and precautions (see also ADDITIONAL SAFETY INFORMATION)

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: Panel A320
UDI-DI code: 04251342603206
Basic UDI-DI: B-04251342603206
Reference / catalog number: 0320
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: AllergyScreen®/AlleisaScreen® is an immunoblot assay for the semi-quantitative determination of allergen-specific immunoglobulin E (IgE) circulating in human serum/plasma.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

W01020205IMMUNOGLOBULIN E - SCREEN

Compliance flags

Safety

Sterile

Single use

Direct marking

Regulatory

Sterilization

Lifecycle

New device

UDI-PI traceability

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Software identification

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.