← Back to catalogue

LabDisk-Analyzer

EUDAMED

Class A (EU MDR)

Ref ESDR12-MB-1000

by Dermagnostix GmbH

Identity

Device Name
LabDisk-Analyzer EUDAMED
Model / Reference
ESDR12-MB-1000 EUDAMED

Identifiers

Primary DI / UDI-DI
04262367270007 EUDAMED
Basic UDI-DI
426236727TD-AZ001GB EUDAMED
Direct Marketing DI
04262367270007 EUDAMED
EMDN Code
W02050199 NUCLEIC ACID TESTING INSTRUMENTS EXCEPT MICRO-ARRAYS - OTHER EUDAMED

Classification

Device Class
Class A EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Microbial Substances

No

EUDAMED

Reagent

No

EUDAMED

Self Testing

No

EUDAMED

Near-Patient Testing

No

EUDAMED

Professional Testing

Yes

EUDAMED

Companion Diagnostics

No

EUDAMED

Surgical Instrument

Yes

EUDAMED

New Device

Yes

EUDAMED

LabDisk-Analyzer by Dermagnostix GmbH — Class A — IVDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDR

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Dermagnostix GmbH
EUDAMED SRN
DE-MF-000025137

Sources (1)

  • EUDAMED 9f3d9c76-ba8d-4712-9a7c-13b4d65dc660 61 fields · synced Jul 16, 2026