Symphony Oct System
EUDAMEDFDA UDIFDA 510(k)Class IIa (EU MDR)
Identity
- Trade Name
- SYMPHONY OCT SYSTEM EUDAMEDSYMPHONY FDA UDI
- Generic Name
- Surgical screwdriver, reusable FDA UDI
- Device Name
- SYMPHONY Navigation Ready Drill Guide Body Drill Trocar Probe Tap Screw Driver Sleeve EUDAMEDSYMPHONY OCT SYSTEM POLYAXIAL SCREW DRIVER SHAFT X20 FDA UDI
- Model / Reference
- SYMPHONY Navigation Ready Instruments Surgical Navigation Instrument EUDAMED2020-33-400 EUDAMEDFDA UDI
- Description
- SYMPHONY OCT SYSTEM POLYAXIAL SCREW DRIVER SHAFT X20 FDA UDI
Identifiers
- Catalog Number
- 202033400 FDA UDI
- Primary DI / UDI-DI
- 10705034530994 EUDAMEDFDA UDI
- Basic UDI-DI
- 0705034a000145F EUDAMED
- Direct Marketing DI
- 10705034530994 EUDAMED
- 510(k) Number
- K191943 FDA UDI
- FDA Product Code
- OLO FDA UDIHXX FDA UDI
- EMDN Code
- Z12130480 STEREOTACTIC ORTHOPAEDIC SURGERY INSTRUMENTS - HARDWARE ACCESSORIES EUDAMED
- GMDN Term
- Surgical screwdriver, reusable FDA UDI
Classification
- Device Class
- Class IIa EUDAMEDClass II FDA UDI
- Regulation Number
- 882.4560 FDA UDI888.4540 FDA UDI
- Market of Registration
- Belgium EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
Single Use
No
Implantable
No
Reusable
Yes
Contains Latex
No
Reprocessed
No
CMR Substance
No
Human-derived
No
Human Tissues
No
Animal Tissues
No
Endocrine Disruptor
No
Administering Medicine
No
Measuring Function
No
Incorporates Medicinal Product
No
Prescription Use
Yes
Over-the-Counter
No
Convenience Kit
No
Combination Product
No
HCT/P
No
Premarket Exempt
No
Lot / Batch Number
Yes
Serial Number
No
Expiration Date
No
Manufacturing Date
No
Category: Multi-purpose stereotactic surgery system
Symphony Oct System by Medos International Sarl — Class IIa — FDA_510K, MDR — listed in EUDAMED, FDA GUDID, FDA 510(k) — regulatory data on deviCERTS
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Authorization Coverage (2 countries)
Regulatory Authorizations
FDA_510K
CE/MDR
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA 510(k) | United States | FDA_510K | K260240 | Class IIa | Active |
| EUDAMED | European Union | CE/MDR | 0705034a000145F | Class IIa | Active |
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Manufacturer
- Manufacturer
- Medos International SARL
- EUDAMED SRN
- CH-MF-000014268
- Authorised Representative
- DePuy Ireland UC IE-AR-000009328
Sources (3)
- EUDAMED 2218db90-c845-4020-9dea-b7878481ab36 61 fields · synced Jul 15, 2026
- FDA UDI 645b8166-9e54-4f73-a3d2-db77b63c5305 36 fields · synced May 29, 2026
- FDA 510(k) K260240 1 fields · synced May 18, 2026