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Inion S-1™ Instrumentation

EUDAMED

Class I (EU MDR)

Ref ACC-9841

by Inion Oy

Identity

Trade Name
Inion S-1™ Instrumentation EUDAMED
Inion S-1 Instrumentation EUDAMED
Device Name
Inion S-1 Instruments EUDAMED
Inion Instruments EUDAMED
Model / Reference
ACC-9841 EUDAMED

Identifiers

Primary DI / UDI-DI
06438408004872 EUDAMED
Basic UDI-DI
B-06438408004872 EUDAMED
6438408INION-IM-INSTRUM68 EUDAMED
Secondary DI
M224ACC984110 EUDAMED
EMDN Code
V0402 CLINICAL USE TRAYS AND BOWLS 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 S-1™ Instrumentation by Inion Oy — Class I — MDR, MDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

European Union Active

CE/MDD

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Manufacturer

Manufacturer
Inion Oy
EUDAMED SRN
FI-MF-000000646

Sources (2)

  • EUDAMED 330fa7e4-b093-482b-84c6-b82edf62fde2 61 fields · synced Oct 1, 2026
  • EUDAMED 797c2e61-a294-4d11-8d7e-f53ac82e6781 61 fields · synced May 19, 2026