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Surgitron 4.0 Dual Rf 120
EUDAMEDFDA UDIClass IIb (EU MDR)
Ref IEC3A-S30Model IEC3A-S30
by Cynosure LLC
Identity
- Trade Name
- SURGITRON 4.0 DUAL RF 120 EUDAMEDFDA UDI
- Generic Name
- Electrosurgical system FDA UDI
- Device Name
- SURGITRON 4.0 DUAL RF 120 EUDAMEDSURGITRON 4.0 DUAL RF/120 IEC FDA UDI
- Model / Reference
- IEC3A-S30 EUDAMEDFDA UDI
- Description
- SURGITRON 4.0 DUAL RF/120 IEC FDA UDI
Identifiers
- Catalog Number
- IEC3A-S30 FDA UDI
- Primary DI / UDI-DI
- 00841494104870 EUDAMEDFDA UDI
- Basic UDI-DI
- B-00841494104870 EUDAMED
- 510(k) Number
- K013255 FDA UDI
- FDA Product Code
- GEI FDA UDI
- EMDN Code
- K02030199 RADIOFREQUENCY SURGERY INSTRUMENTS, SINGLE-USE - OTHER EUDAMED
- GMDN Term
- Electrosurgical system FDA UDI
Classification
- Device Class
- Class IIb EUDAMEDClass II FDA UDI
- Regulation Number
- 878.4400 FDA UDI
- Market of Registration
- Netherlands EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
EUDAMEDFDA UDI
Single Use
No
FDA UDI
Implantable
No
EUDAMEDFDA UDI
Reusable
No
EUDAMED
Contains Latex
No
EUDAMEDFDA UDI
Reprocessed
No
EUDAMED
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
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
No
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Microwave ablation system probe, non-powered
Surgitron 4.0 Dual Rf 120 by Cynosure, LLC — Class IIb — MDD, 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/MDD
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDD | B-00841494104870 | Class IIb | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class IIb | Pending data |
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Manufacturer
- Manufacturer
- Cynosure LLC
- EUDAMED SRN
- US-MF-000010200
- Authorised Representative
- Cynosure B.V. NL-AR-000009566
Sources (2)
- EUDAMED 92e1cb77-f640-4dd5-8fe7-0451ec6fef65 61 fields · synced May 31, 2026
- FDA UDI 6ec75221-0d95-432d-9140-a5c896d7010f 35 fields · synced May 27, 2026