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Guided Stem Impactor

EUDAMED

Class I (EU MDR)

Ref 800266

by Atesos medical AG

Identity

Trade Name
Guided Stem Impactor EUDAMED
Device Name
Schafteinschläger geführt EUDAMED
Model / Reference
800266 EUDAMED

Identifiers

Primary DI / UDI-DI
07640164282862 EUDAMED
Basic UDI-DI
B-07640164282862 EUDAMED
EMDN Code
L091104 ORTHOPAEDIC PROSTHESES POSITIONERS, REUSABLE 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

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Guided Stem Impactor by Atesos medical AG — Class I — MDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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Manufacturer

Manufacturer
Atesos medical AG
EUDAMED SRN
CH-MF-000010304
Authorised Representative
hestomed GmbH DE-AR-000006853

Sources (1)

  • EUDAMED ff5a87cf-5349-4466-9d0c-3c0087e3afbb 61 fields · synced Jun 19, 2026