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Any-Seal RC

EUDAMED

Class IIa (EU MDR)

Ref GB2021OC005(012022)Model AS10GBX1S, 503-1 Any-Seal RC

by MEDICLUS Co., Ltd.

Identity

Trade Name
Any-Seal RC EUDAMED
Device Name
Any-Seal RC EUDAMED
Model / Reference
AS10GBX1S, 503-1 Any-Seal RC EUDAMED
GB2021OC005(012022) EUDAMED

Identifiers

Primary DI / UDI-DI
08809518341160 EUDAMED
Basic UDI-DI
B-08809518341160 EUDAMED
EMDN Code
Q01010299 ROOT CANAL FILLING DEVICES - OTHER EUDAMED

Classification

Device Class
Class IIa 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

Any-Seal RC by MEDICLUS Co., Ltd. — Class IIa — 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
MEDICLUS Co., Ltd.
EUDAMED SRN
KR-MF-000022584
Authorised Representative
KTR Europe GmbH DE-AR-000005685

Sources (1)

  • EUDAMED f7c06916-62a4-453f-88d0-4fb8af9dc68b 61 fields · synced Aug 1, 2026