Identity
- Trade Name
- Sonata® System Radiofrequency Generator FDA UDI
- Generic Name
- Ultrasound-guided intrauterine radio-frequency ablation system generator FDA UDI
- Device Name
- Ultrasound-guided intrauterine electrosurgical system generator FDA UDI
- Model / Reference
- RFG2-110 FDA UDI
- Description
- Ultrasound-guided intrauterine electrosurgical system generator FDA UDI
Identifiers
- Catalog Number
- RFG2-110 FDA UDI
- Primary DI / UDI-DI
- 10817929020203 FDA UDI
- 510(k) Number
- K173703 FDA UDI
- FDA Product Code
- IYO FDA UDIKNF FDA UDI
- GMDN Term
- Ultrasound-guided intrauterine radio-frequency ablation system generator FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 892.1560 FDA UDI884.4160 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
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: Ultrasound-guided intrauterine radio-frequency ablation system generator
Sonata® System Radiofrequency Generator by Gynesonics, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
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Manufacturer
- Manufacturer
- Gynesonics, Inc.
Sources (1)
- FDA UDI ea87d0f4-c4e0-482d-8421-bd912a80ca2b 37 fields · synced May 30, 2026