← Back to catalogue

Inion CPS/OTPS Instrumentation

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref INS-9003

by Inion Oy

Identity

Trade Name
Inion CPS/OTPS Instrumentation EUDAMED
Inion CPS™/OTPS™ instrumentation FDA UDI
Generic Name
Fluted surgical drill bit, reusable FDA UDI
Device Name
Inion Instruments EUDAMED
Inion CPS/OTPS instrumentation EUDAMED
1.60 mm drill bit with 7 mm stop (J-latch) FDA UDI
Model / Reference
INS-9003 EUDAMED
1 FDA UDI
Description
1.60 mm drill bit with 7 mm stop (J-latch) FDA UDI

Identifiers

Catalog Number
INS-9003 FDA UDI
Primary DI / UDI-DI
06438408000256 EUDAMEDFDA UDI
Basic UDI-DI
6438408INION-IIA-INSTRUUR EUDAMED
B-06438408000256 EUDAMED
Secondary DI
M224INS900310 EUDAMED
FDA Product Code
HTW FDA UDI
EMDN Code
L091001 INSTRUMENTS FOR INSERTION AND EXTRACTION OF MATERIALS FOR OSTEOSYNTHESIS, REUSABLE EUDAMED
GMDN Term
Fluted surgical drill bit, reusable FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class I FDA 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 CPS/OTPS 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 5c21b136-7010-499f-9761-d8948518cb0d 61 fields · synced Jul 29, 2026
  • EUDAMED 3eb118d8-91e8-47b6-a4b9-ef160e9fde89 61 fields · synced May 19, 2026
  • FDA UDI afb09174-f29d-44da-ac65-ba259beb94fc 34 fields · synced May 30, 2026