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Aegis Anterior Lumbar Plate
EUDAMEDFDA UDIClass I (EU MDR)
Ref 287110115Model AEGIS Anterior Lumbar Plate Cutting Instruments
Identity
- Trade Name
- AEGIS ANTERIOR LUMBAR PLATE EUDAMEDAEGIS FDA UDI
- Generic Name
- Bone awl, reusable FDA UDI
- Device Name
- AEGIS Awl EUDAMEDAEGIS ANTERIOR LUMBAR PLATE AWL, FIXED FDA UDI
- Model / Reference
- AEGIS Anterior Lumbar Plate Cutting Instruments EUDAMED287110115 EUDAMEDFDA UDI
- Description
- AEGIS ANTERIOR LUMBAR PLATE AWL, FIXED FDA UDI
Identifiers
- Catalog Number
- 287110115 FDA UDI
- Primary DI / UDI-DI
- 10705034218168 EUDAMEDFDA UDI
- Basic UDI-DI
- 0705034a000996H EUDAMED
- Direct Marketing DI
- 10705034218168 EUDAMED
- FDA Product Code
- HWJ FDA UDI
- EMDN Code
- L090999 ORTHOPAEDIC SURGERY CUTTING INSTRUMENTS, REUSABLE - OTHER EUDAMED
- GMDN Term
- Bone awl, 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
Aegis Anterior Lumbar Plate 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 | 0705034a000996H | 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 8690b8df-c429-4f9b-8d5e-df417c74af2d 61 fields · synced Jul 23, 2026
- FDA UDI 75022bf9-eadf-4851-a3b4-0d0ab47ef2a7 35 fields · synced May 29, 2026