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Astodia

EUDAMED

Class I (EU MDR)

Ref DIA120

by Stihler Electronic GmbH

Identity

Trade Name
ASTODIA EUDAMED
Device Name
ASTODIA EUDAMED
Model / Reference
DIA120 EUDAMED

Identifiers

Primary DI / UDI-DI
04260114140856 EUDAMED
Basic UDI-DI
426011414DIA8J EUDAMED
Direct Marketing DI
04260114140856 EUDAMED
EMDN Code
Z110702 DIAPHANOSCOPE EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Astodia by Stihler Electronic Gmbh — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
DE-MF-000006188

Sources (1)

  • EUDAMED 37ed2aee-26fd-400d-9b5e-1de01e306b32 61 fields · synced Jul 16, 2026