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Volus 10™

EUDAMED

Class III (EU MDR)

Ref VOLUS 10™

by Across Co., Ltd.

Identity

Device Name
VOLUS 10™ EUDAMED
Model / Reference
VOLUS 10™ EUDAMED

Identifiers

Primary DI / UDI-DI
D-88094270404659E EUDAMED
Basic UDI-DI
B-88094270404659E EUDAMED
EMDN Code
P900402 RESORBABLE FILLING AND RECONSTRUCTION DEVICES EUDAMED

Classification

Device Class
Class III EUDAMED
Market of Registration
Bulgaria EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Implantable

Yes

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

Volus 10™ by Across Co., Ltd. — Class III — 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
Across Co., Ltd.
EUDAMED SRN
KR-MF-000012936
Authorised Representative
JaviTech e.K. DE-AR-000005875

Sources (1)

  • EUDAMED 93dab5b3-7682-4c6b-8f9c-4b316b20ff11 61 fields · synced Jun 18, 2026