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Orbis

EUDAMED

Class I (EU MDR)

Ref PLANDENT400R-B

by Akzenta International SA

Identity

Trade Name
ORBIS EUDAMED
Device Name
MICRO APPLICATORS EUDAMED
Model / Reference
PLANDENT400R-B EUDAMED

Identifiers

Primary DI / UDI-DI
04250476618094 EUDAMED
Basic UDI-DI
42504766MICUL EUDAMED
EMDN Code
Q019006 DENTAL MATERIAL APPLICATION TIPS AND BRUSHES, SINGLE-USE EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Finland EUDAMED

Clinical & Handling

Sterile

No

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

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Orbis by Akzenta International SA — Class I — 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
CH-MF-000036434
Authorised Representative
IQX GmbH AT-AR-000016713

Sources (1)

  • EUDAMED 7d5d63fa-0b57-407f-af1c-1571abc3e08c 61 fields · synced Jun 18, 2026