← Back to catalogue

Inion Hexalon™ Instrumentation

EUDAMEDFDA UDI

Class I (EU MDR)

Ref INS-9207Ref INS-9200

by Inion Oy

Identity

Trade Name
Inion Hexalon™ Instrumentation EUDAMEDFDA UDI
Generic Name
Orthopaedic bur, reusable FDA UDI
Device Name
Inion Hexalon Instrument EUDAMED
RapidNotcher FDA UDI
Model / Reference
INS-9207 EUDAMED
INS-9200 EUDAMED
2 FDA UDI
Description
RapidNotcher FDA UDI

Identifiers

Catalog Number
INS-9207 FDA UDI
Primary DI / UDI-DI
06438408012020 EUDAMEDFDA UDI
06438408012037 EUDAMED
Basic UDI-DI
6438408HEXALONINSTIR54 EUDAMED
Direct Marketing DI
06438408012020 EUDAMED
06438408012037 EUDAMED
FDA Product Code
LXH FDA UDI
EMDN Code
L091001 INSTRUMENTS FOR INSERTION AND EXTRACTION OF MATERIALS FOR OSTEOSYNTHESIS, REUSABLE EUDAMED
GMDN Term
Orthopaedic bur, reusable FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
888.4540 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

Yes

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 Hexalon™ Instrumentation by Inion Oy — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

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 f5741912-a5ad-417c-a424-0a3263ed2d87 61 fields · synced Jul 16, 2026
  • EUDAMED 6c6603cf-691b-4606-bffe-71312f7dc450 61 fields · synced May 19, 2026
  • FDA UDI f52eac90-431f-4316-aa31-c80e33f98483 34 fields · synced May 30, 2026