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Remo-Wax korvatipat 10 ml

EUDAMED

Class IIa (EU MDR)

Ref 112116

by Orion Oyj

Identity

Trade Name
Remo-Wax korvatipat 10 ml EUDAMED
Remo-Wax EUDAMED
Device Name
Remo-Wax EUDAMED
Model / Reference
112116 EUDAMED

Identifiers

Primary DI / UDI-DI
06432100002495 EUDAMED
Basic UDI-DI
643210REM001UD EUDAMED
B-06432100002495 EUDAMED
EMDN Code
Q030499 OTOLOGY DEVICES - OTHER EUDAMED

Classification

Device Class
Class IIa EUDAMED
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

Remo-Wax korvatipat 10 ml by Orion Oyj — Class IIa — MDD, MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

European Union Active

CE/MDR

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Manufacturer

Manufacturer
Orion Oyj
EUDAMED SRN
FI-MF-000001595

Sources (2)

  • EUDAMED e171aed4-0aea-4184-bd70-fe97e1c51a8a 61 fields · synced Jul 27, 2026
  • EUDAMED c200fc83-2057-4a75-a058-7589888967d5 61 fields · synced May 18, 2026