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OrthoPulse®

EUDAMED

Class IIa (EU MDR)

Ref OPi2E-100

by Biolux Technology GmbH

Identity

Trade Name
OrthoPulse® EUDAMED
Device Name
OrthoPulse 2.0E EUDAMED
Model / Reference
OPi2E-100 EUDAMED

Identifiers

Primary DI / UDI-DI
D-9120118090074T7 EUDAMED
Basic UDI-DI
B-9120118090074T7 EUDAMED
EMDN Code
Q010499 ORTHODONTIC 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

OrthoPulse® by Biolux Technology Gmbh — 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

EUDAMED SRN
AT-MF-000020789

Sources (1)

  • EUDAMED d76d8f24-72ca-40d1-85b8-25d405ca1b8d 61 fields · synced May 23, 2026