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Targis

FDA UDI

Class III (US FDA UDI)

by Urologix, Inc.

Identity

Trade Name
Targis FDA UDI
Generic Name
Microwave hyperthermia system applicator, intracorporeal FDA UDI
Device Name
RTU Plus Reusable Handle, 1 pack FDA UDI
Model / Reference
RB3131A FDA UDI
Description
RTU Plus Reusable Handle, 1 pack FDA UDI

Identifiers

Primary DI / UDI-DI
M876RB3131A1 FDA UDI
FDA Product Code
MEQ FDA UDI
GMDN Term
Microwave hyperthermia system applicator, intracorporeal FDA UDI

Classification

Device Class
Class III FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
High-level Disinfectant FDA UDI

Category: Microwave hyperthermia system applicator, intracorporeal

Targis by Urologix, Inc. — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Microwave hyperthermia system applicator, intracorporeal.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Urologix, Inc.

Sources (1)

  • FDA UDI 48df553a-1f6d-446a-9d1b-3e40f4988ead 33 fields · synced May 30, 2026