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Inion S-1 Instrumentation

EUDAMED

Class I (EU MDR)

Ref ACC-9831

by Inion Oy

Identity

Trade Name
Inion S-1 Instrumentation EUDAMED
Inion S-1™ Instrumentation EUDAMED
Device Name
Inion Instruments EUDAMED
Inion S-1 Instruments EUDAMED
Model / Reference
ACC-9831 EUDAMED

Identifiers

Primary DI / UDI-DI
06438408004834 EUDAMED
Basic UDI-DI
6438408INION-IR-INSTRUM9T EUDAMED
B-06438408004834 EUDAMED
Secondary DI
M224ACC983110 EUDAMED
EMDN Code
L091002 INSTRUMENTS FOR PROCESSING MATERIALS FOR OSTEOSYNTHESIS, REUSABLE 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

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Category: Wire holding/twisting forceps

Inion S-1 Instrumentation by Inion Oy — Class I — MDD, MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Wire holding/twisting forceps.

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 9f27602a-c287-4af8-93b1-38be9143b01d 61 fields · synced Jun 20, 2026
  • EUDAMED 00aa3b61-9f86-4ed1-b7e5-0565f8cfd9f3 61 fields · synced May 19, 2026