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Expedium Spine System
EUDAMEDFDA UDIClass I (EU MDR)
Ref 299704310Model Expedium Verse Reusable Instruments
Identity
- Trade Name
- EXPEDIUM SPINE SYSTEM EUDAMEDEXPEDIUM FDA UDI
- Generic Name
- Orthopaedic implant impactor, reusable FDA UDI
- Device Name
- Expedium Rod Clamp Compressor EUDAMEDEXPEDIUM SPINE SYSTEM TAB BREAKER, BODY FDA UDI
- Model / Reference
- Expedium Verse Reusable Instruments EUDAMED299704310 EUDAMEDFDA UDI
- Description
- EXPEDIUM SPINE SYSTEM TAB BREAKER, BODY FDA UDI
Identifiers
- Catalog Number
- 299704310 FDA UDI
- Primary DI / UDI-DI
- 10705034467375 EUDAMEDFDA UDI
- Basic UDI-DI
- 0705034a001145L EUDAMED
- Direct Marketing DI
- 10705034467375 EUDAMED
- FDA Product Code
- LXH FDA UDI
- EMDN Code
- L090999 ORTHOPAEDIC SURGERY CUTTING INSTRUMENTS, REUSABLE - OTHER EUDAMED
- GMDN Term
- Orthopaedic implant impactor, reusable FDA UDI
Classification
- Device Class
- Class I EUDAMEDFDA UDI
- Regulation Number
- 888.4540 FDA UDI
- Market of Registration
- Belgium 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
Yes
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
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Category: Bone cutting forceps, reusable
Expedium Spine System by Medos International Sarl — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS
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Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Active
CE/MDR
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | 0705034a001145L | Class I | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- Medos International SARL
- EUDAMED SRN
- CH-MF-000014268
- Authorised Representative
- DePuy Ireland UC IE-AR-000009328
Sources (2)
- EUDAMED e73e28df-af93-4325-b60f-34dc629b9bca 61 fields · synced May 30, 2026
- FDA UDI b589f3a9-4297-4cea-88c9-90218019911b 35 fields · synced May 30, 2026