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Minitouch

FDA UDI

Class III (US FDA UDI)

by Microcube, LLC

Identity

Trade Name
Minitouch FDA UDI
Generic Name
Microwave ablation system FDA UDI
Device Name
Central Unit FDA UDI
Model / Reference
4002 FDA UDI
Description
Central Unit FDA UDI

Identifiers

Primary DI / UDI-DI
00850044503117 FDA UDI
PMA Number
P230002 FDA UDI
FDA Product Code
MNB FDA UDI
GMDN Term
Microwave ablation system FDA UDI

Classification

Device Class
Class III 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
MRI Safety
MR Unsafe FDA UDI

Category: Microwave ablation system

Minitouch by Microcube, LLC — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Microwave ablation system.

Cleared under the same submission

P230002 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Microcube, LLC

Sources (1)

  • FDA UDI 591401fd-6b8e-423e-b04d-49de662beb7d 34 fields · synced Jun 8, 2026