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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

102308 — IVDR Class A IVDR by BIOMED Labordiagnostik…

MD Atlas
BIOMED Labordiagnostik GmbH

EUDAMED last updated this device on May 21, 2026

102308

426048108STA00537K

On the marketIVDR Class A

Applicable legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Organization name: BIOMED Labordiagnostik GmbH
UDI-DI code: 04260481081967
Reference / catalog number: 102308

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Manufacturer information

Organization name: BIOMED Labordiagnostik GmbH
SRN: DE-MF-000010310
Manufacturer status: Active

Related devices

102307426048108STA00537KOn the market 102301426048108STA00517FOn the market 102302426048108STA00517FOn the market 102313426048108STA00547MOn the market 102314426048108STA00547MOn 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

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

CW010
EUDAMED did not publish a description for this code.
CW032
EUDAMED did not publish a description for this code.
CW018
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: 04260481081967
Basic UDI-DI: 426048108STA00537K
Reference / catalog number: 102308
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: 1
Additional product description: —
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

W0103010302ROMANOWSKY STAINS

Compliance flags

Safety

Sterile

Single use

Direct marking

Regulatory

Sterilization

Lifecycle

New device

UDI-PI traceability

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Software identification