← Back to catalogue
Inion FreedomScrew Instrumentation
EUDAMEDFDA UDIClass IIa (EU MDR)
Ref IFS-4508
by Inion Oy
Identity
- Trade Name
- Inion FreedomScrew Instrumentation EUDAMEDInion FreedomScrew instruments FDA UDI
- Generic Name
- Bone tap, reusable FDA UDI
- Device Name
- Inion Instruments EUDAMEDInion FreedomScrew instrumentation EUDAMEDDrill tap Ø4.5 mm, cannulated FDA UDI
- Model / Reference
- IFS-4508 EUDAMED1 FDA UDI
- Description
- Drill tap Ø4.5 mm, cannulated FDA UDI
Identifiers
- Catalog Number
- IFS-4508 FDA UDI
- Primary DI / UDI-DI
- 06438408003783 EUDAMEDFDA UDI
- Basic UDI-DI
- 6438408INION-IIA-INSTRUUR EUDAMEDB-06438408003783 EUDAMED
- Secondary DI
- M224IFS450810 EUDAMED
- FDA Product Code
- HWX FDA UDI
- EMDN Code
- L098003 ORTHOPAEDIC AND TRAUMATOLOGICAL SURGERY TAPS, REUSABLE EUDAMED
- GMDN Term
- Bone tap, reusable FDA UDI
Classification
- Device Class
- Class IIa EUDAMEDClass 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
Moist Heat or Steam Sterilization FDA UDI
Inion FreedomScrew 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
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDD | 6438408INION-IIA-INSTRUUR | Class IIa | Active |
| EUDAMED | European Union | CE/MDR | 6438408INION-IIA-INSTRUUR | Class IIa | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class IIa | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Inion Oy
- EUDAMED SRN
- FI-MF-000000646
Sources (3)
- EUDAMED b86cdbfb-bbe7-4171-96c1-d4a65cc1e9dc 61 fields · synced Jun 19, 2026
- EUDAMED a8a1973a-3a32-4462-8e07-c6b5b8c6c087 61 fields · synced May 19, 2026
- FDA UDI 3d593a46-15df-46a5-95da-f3d15424b940 34 fields · synced May 30, 2026