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Inion Universal Instruments

EUDAMED

Class I (EU MDR)

Ref ACC-9805Ref ACC-9805

by Inion Oy

Identity

Trade Name
Inion Universal Instruments EUDAMED
Device Name
Inion Instruments EUDAMED
Inion Universal instrument EUDAMED
Model / Reference
ACC-9805 EUDAMED

Identifiers

Primary DI / UDI-DI
06438408002113 EUDAMED
Basic UDI-DI
6438408INION-IM-INSTRUM68 EUDAMED
B-06438408002113 EUDAMED
Secondary DI
M224ACC98059 EUDAMED
EMDN Code
V0402 CLINICAL USE TRAYS AND BOWLS EUDAMED
S010401 TRAYS, BASKETS, TUBS FOR STERILISATION AND THEIR COMPONENTS EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Finland EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

Yes

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

Yes

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Inion Universal Instruments by Inion Oy — Class I — 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
Inion Oy
EUDAMED SRN
FI-MF-000000646

Sources (2)

  • EUDAMED 0d023dea-7e0f-42ee-9719-b047f5d73439 61 fields · synced May 24, 2026
  • EUDAMED bdcbc0a4-c365-42c8-a248-e4e71cfc7a03 61 fields · synced May 19, 2026