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Astotube

EUDAMED

Class IIa (EU MDR)

Ref M77455502

by Stihler Electronic GmbH

Identity

Trade Name
ASTOTUBE EUDAMED
Device Name
ASTOTUBE M77455502 EUDAMED
Model / Reference
M77455502 EUDAMED

Identifiers

Primary DI / UDI-DI
04260114141396 EUDAMED
Basic UDI-DI
426011414TUBE5P EUDAMED
Unit of Use DI
04260114141433 EUDAMED
EMDN Code
A03020199 EXTENSIONS - OTHER EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

Yes

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

Yes

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Astotube by Stihler Electronic Gmbh — Class IIa — 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 4a232115-249e-43eb-bf34-10e4aee386db 61 fields · synced May 24, 2026