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Inion S-1™ Instrumentation

EUDAMED

Class I (EU MDR)

Ref ACC-9832

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-9832 EUDAMED

Identifiers

Primary DI / UDI-DI
06438408004841 EUDAMED
Basic UDI-DI
B-06438408004841 EUDAMED
6438408INION-IR-INSTRUM9T EUDAMED
Secondary DI
M224ACC983210 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 — MDR, MDD — 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/MDR

European Union Active

CE/MDD

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Manufacturer

Manufacturer
Inion Oy
EUDAMED SRN
FI-MF-000000646

Sources (2)

  • EUDAMED b2c0cb28-328e-431c-8554-0e175d55084a 61 fields · synced Jun 18, 2026
  • EUDAMED a1cb6bcd-6e94-4092-a95b-525150009682 61 fields · synced May 19, 2026