Identity
- Trade Name
- Sonachill FDA UDI
- Generic Name
- Ultrasonic hyperthermia system FDA UDI
- Device Name
- System used to regulate temperature and oxygen content of sterile water for a procedure. FDA UDI
- Model / Reference
- 102-17000-0007 FDA UDI
- Description
- System used to regulate temperature and oxygen content of sterile water for a procedure. FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00868108000274 FDA UDI
- FDA Product Code
- PLP FDA UDI
- GMDN Term
- Ultrasonic hyperthermia system FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 876.4340 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: Ultrasonic hyperthermia system
Sonachill by Focus Surgery, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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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
- Focus Surgery, Inc.
Sources (1)
- FDA UDI 226ae912-8e3f-40a8-9ff6-27e2726417f2 34 fields · synced Jun 1, 2026