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Trial shell size 50

EUDAMED

Class I (EU MDR)

Ref 800036

by Atesos medical AG

Identity

Device Name
Trial shell size 50 EUDAMED
Model / Reference
800036 EUDAMED

Identifiers

Primary DI / UDI-DI
07640164281742 EUDAMED
Basic UDI-DI
B-07640164281742 EUDAMED
EMDN Code
L091199 ORTHOPAEDIC PROSTHETICS INSTRUMENTS, REUSABLE - OTHER EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

Yes

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

Trial shell size 50 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 5ab6e4ea-faae-425c-af4e-5cad5067ef48 61 fields · synced Oct 7, 2026