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Targis RB3131A

by Urologix, Inc. 2 variants

Targis RB3131A is a Class III device made by Urologix, Inc., listed in FDA GUDID since 26 Sep 2014 (UDI-DI M876RB3131A2), registry data as of 23 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing NumberM876RB3131A2 UDI-DI Date26 Sep 2014ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
Targis
Generic name
Microwave hyperthermia system applicator, intracorporeal
Model / reference
RB3131A
Primary DI / UDI-DI
M876RB3131A2
FDA product code
MEQ
GMDN term
Microwave hyperthermia system applicator, intracorporeal
Device class
Class III
GUDID distribution status
In Commercial Distribution
Sterilisation method
High-level Disinfectant

Related devices

Category: Microwave hyperthermia system applicator, intracorporeal

Similar devices

Other devices filed under FDA product code MEQ (System, Hyperthermia, Rf/Microwave (Benign Prostatic Hyperplasia),Thermotherapy).

Other devices from Urologix, Inc.

See all devices from Urologix, Inc. →

Properties

  • Supplied sterile
  • Sterilise before use
  • Lot / batch number
  • Expiration date
Other properties (11, all answered No)