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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

K5004DBS — IVDD — General IVDD by Immundiagnostik AG

MD Atlas
Immundiagnostik AG

EUDAMED last updated this device on May 19, 2026

K5004DBS

B-04050598008823

On the marketIVDD — General

Applicable legislation: IVDD [Directive 98/79/EC on in vitro diagnostic medical devices]
Organization name: Immundiagnostik AG
UDI-DI code: 04050598008823
Reference / catalog number: K5004DBS

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Manufacturer information

Organization name: Immundiagnostik AG
SRN: DE-MF-000020905
Manufacturer status: Active

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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.

Critical warnings

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

CW018
EUDAMED did not publish a description for this code.
CW043
EUDAMED did not publish a description for this code.
CW081
EUDAMED did not publish a description for this code.
CW083
EUDAMED did not publish a description for this code.
CW085
EUDAMED did not publish a description for this code.

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: not provided
UDI-DI code: 04050598008823
Basic UDI-DI: B-04050598008823
Reference / catalog number: K5004DBS
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: IDK® anti-SARS-CoV-2 IgG is an enzyme-linked immunosorbent assay (ELISA) for quantitative measurement of IgG antibodies (including neutralizing antibodies) against the novel coronavirus SARS-CoV-2 in human dry blood spot samples. The assay is an in vitro diagnostic medical device and is intended to be used by professional users in a laboratory environment. This ELISA can be performed manually or using an automated platform. This test serves as complement to infection diagnosis and is used for the detection of IgG antibodies after a previous infection with SARS-CoV-2 or after COVID-19 vaccination.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

W0105041103CORONAVIRUS IGG

Compliance flags

Safety

Sterile

Single use

Direct marking

Regulatory

Sterilization

Lifecycle

New device

UDI-PI traceability

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