Identity
- Trade Name
- NEUWAVE FDA UDI
- Generic Name
- Microwave ablation system generator FDA UDI
- Device Name
- NEUWAVE Flex MAS, 220-230VAC FDA UDI
- Model / Reference
- DR-000894 FDA UDI
- Description
- NEUWAVE Flex MAS, 220-230VAC FDA UDI
Identifiers
- Catalog Number
- DR-000894 FDA UDI
- Primary DI / UDI-DI
- 00818913020189 FDA UDI
- 510(k) Number
- K163118 FDA UDI
- FDA Product Code
- NEY FDA UDI
- GMDN Term
- Microwave ablation system generator FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 878.4400 FDA UDI
- Commercial Distribution
- Not 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
MR Unsafe FDA UDI
Neuwave by NeuWave Medical, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Cleared under the same submission
K163118 also covers:
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
- NeuWave Medical, Inc.
Sources (1)
- FDA UDI e0919e45-f584-41f9-a7d8-0b4c4071da0e 38 fields · synced Jun 8, 2026