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Therabionic P1

FDA UDI

by TheraBionic GmbH

Identity

Trade Name
Therabionic P1 FDA UDI
Generic Name
Alternating electric field antimitotic cancer treatment system generator FDA UDI
Device Name
AC power supply unit, 15W for the TheraBionic P1 - Variant 2 FDA UDI
Model / Reference
02 FDA UDI
Description
AC power supply unit, 15W for the TheraBionic P1 - Variant 2 FDA UDI

Identifiers

Catalog Number
THBC P1-PS-02 FDA UDI
Primary DI / UDI-DI
04251867200119 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

Similar devices

Also classified as Alternating electric field antimitotic cancer treatment system generator.

Cleared under the same submission

H220001 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
TheraBionic GmbH

Sources (1)

  • FDA UDI e821839b-07e5-4faa-83b3-e5572265a517 37 fields · synced Jun 8, 2026