Identity
- Trade Name
- TheraBionic P1 FDA UDI
- Generic Name
- Alternating electric field antimitotic cancer treatment system generator FDA UDI
- Device Name
- Patient spoon with connecting cable TheraBionic P1 - Version 4 FDA UDI
- Model / Reference
- THBC P1-S-04 FDA UDI
- Description
- Patient spoon with connecting cable TheraBionic P1 - Version 4 FDA UDI
Identifiers
- Catalog Number
- THBC P1-S-04 FDA UDI
- Primary DI / UDI-DI
- 04251867200126 FDA UDI
- PMA Number
- H220001 FDA UDI
- FDA Product Code
- QOM FDA UDI
- GMDN Term
- Alternating electric field antimitotic cancer treatment system generator FDA UDI
Classification
- 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
Yes
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Alternating electric field antimitotic cancer treatment system generator
TheraBionic P1 by TheraBionic GmbH — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Cleared under the same submission
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 | N/A | Pending data |
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Manufacturer
- Manufacturer
- TheraBionic GmbH
Sources (1)
- FDA UDI ff65b0fb-4657-4426-a728-69028e59be65 37 fields · synced May 30, 2026