← Back to catalogue

Inion CompressOn screw Instrumentation

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref IFS-4018

by Inion Oy

Identity

Trade Name
Inion CompressOn screw Instrumentation EUDAMED
Inion CompressOn™ Instrument FDA UDI
Generic Name
Bone tap, reusable FDA UDI
Device Name
Inion Instruments EUDAMED
Inion CompressOn Screw instrumentation EUDAMED
Drill tap Ø, 4.0 Cannulated, short FDA UDI
Model / Reference
IFS-4018 EUDAMED
1 FDA UDI
Description
Drill tap Ø, 4.0 Cannulated, short FDA UDI

Identifiers

Catalog Number
IFS-4018 FDA UDI
Primary DI / UDI-DI
06438408009716 EUDAMEDFDA UDI
Basic UDI-DI
6438408INION-IIA-INSTRUUR EUDAMED
B-06438408009716 EUDAMED
510(k) Number
K203105 FDA UDI
FDA Product Code
HWC FDA UDI
EMDN Code
L098003 ORTHOPAEDIC AND TRAUMATOLOGICAL SURGERY TAPS, REUSABLE EUDAMED
GMDN Term
Bone tap, reusable FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class II FDA UDI
Regulation Number
888.3040 FDA UDI
Market of Registration
Finland EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

Yes

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

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

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Inion CompressOn screw Instrumentation by Inion Oy — Class IIa — MDD, MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDD

European Union Active

CE/MDR

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Inion Oy
EUDAMED SRN
FI-MF-000000646

Sources (3)

  • EUDAMED b5df710b-b424-4de3-b510-73cec2b87a9e 61 fields · synced Jul 21, 2026
  • EUDAMED 011f87b5-ad9f-4c23-9c91-508e3f1e679b 61 fields · synced May 19, 2026
  • FDA UDI f7a52aae-fe50-4cfd-810c-9aacd8e7e890 35 fields · synced May 22, 2026