← Back to catalogue
Inion ACL Instrumentation
EUDAMEDFDA UDIClass IIa (EU MDR)
Ref INS-9326
by Inion Oy
Identity
- Trade Name
- Inion ACL Instrumentation EUDAMEDInion ACL™ Instrumentation FDA UDI
- Generic Name
- Orthopaedic broach FDA UDI
- Device Name
- Inion Instruments EUDAMEDInion ACL Instrumentation EUDAMEDCannulated headed reamer, 4.5mm FDA UDI
- Model / Reference
- INS-9326 EUDAMED1 FDA UDI
- Description
- Cannulated headed reamer, 4.5mm FDA UDI
Identifiers
- Catalog Number
- INS-9326 FDA UDI
- Primary DI / UDI-DI
- 06438408002731 EUDAMEDFDA UDI
- Basic UDI-DI
- 6438408INION-IIA-INSTRUUR EUDAMEDB-06438408002731 EUDAMED
- Secondary DI
- M224INS93269 EUDAMED
- FDA Product Code
- HTO FDA UDI
- EMDN Code
- L091001 INSTRUMENTS FOR INSERTION AND EXTRACTION OF MATERIALS FOR OSTEOSYNTHESIS, REUSABLE EUDAMED
- GMDN Term
- Orthopaedic broach 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 ACL 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 7720e721-09b8-4dc9-b194-b8cfccdb4820 61 fields · synced Jul 14, 2026
- EUDAMED 564a6c3d-9b11-4b53-bbff-36bc2ff0d27d 61 fields · synced May 17, 2026
- FDA UDI 11c76175-4e20-46a3-9e3b-e47991563d21 34 fields · synced May 30, 2026