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Inion Universal instruments

EUDAMED

Class I (EU MDR)

Ref ACC-9813 Ref ACC-9813

by Inion Oy

Identity

Trade Name
Inion Universal instruments EUDAMED
Device Name
Inion Universal instrument EUDAMED
Inion Instruments EUDAMED
Model / Reference
ACC-9813 EUDAMED

Identifiers

Primary DI / UDI-DI
06438408000362 EUDAMED
Basic UDI-DI
B-06438408000362 EUDAMED
6438408INION-IM-INSTRUM68 EUDAMED
Secondary DI
M224ACC98139 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 Universal instruments 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 4149d52d-76a6-4d66-a29e-185fef596ced 61 fields · synced May 29, 2026
  • EUDAMED e0515622-a5d6-4f7e-b6c7-37e2e3c6d56b 61 fields · synced May 19, 2026