Owl Dtrh-018/80/10

by Diros Technology, Inc.

Owl Dtrh-018/80/10 is a Class II device made by Diros Technology, Inc., listed in FDA GUDID since 1 Sep 2016 (UDI-DI 00825114005174), 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

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number00825114005174 UDI-DI	Date1 Sep 2016Listed	StatusListed GUDID: in commercial distribution

Official records

AccessGUDID record UDI-DI 00825114005174

Coverage

1 jurisdiction

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Withdrawn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-018/80/10
Description: OWL STERILE SINGLE USE DISPOSABLE TRIDENT HYBRID RF INSULATED CANNULA, 18GA, 80MM LONG, 5MM BARE TIP

Primary DI / UDI-DI: 00825114005174
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

Similar devices in this category

Other devices filed under Percutaneous radio-frequency ablation probe cannula, single-use.

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Properties

Supplied sterile
Single use
Prescription use
Lot / batch number
Expiration date
Manufacturing date

Other properties (9, all answered No)