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Owl Dtrh-020/80/5

by Diros Technology, Inc.

Owl Dtrh-020/80/5 is a Class II device made by Diros Technology, Inc., listed in FDA GUDID since 1 Sep 2016 (UDI-DI 00825114004955), 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 Number00825114004955 UDI-DI Date1 Sep 2016ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade name
Owl
Generic name
Percutaneous radio-frequency ablation probe cannula, single-use
Model / Ref / Catalog
DTRH-020/80/5
Description
OWL STERILE SINGLE USE DISPOSABLE TRIDENT HYBRID RF INSULATED CANNULA, 20GA, 80MM LONG, 5MM BARE TIP
Primary DI / UDI-DI
00825114004955
FDA product code
GXI
GMDN term
Percutaneous radio-frequency ablation probe cannula, single-use
Device class
Class II
Regulation number
882.4725
GUDID distribution status
In Commercial Distribution
MRI safety
MR Unsafe

Related devices

Category: Percutaneous radio-frequency ablation probe cannula, single-use

Other devices from Diros Technology, Inc.

See all devices from Diros Technology, Inc. →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (9, all answered No)