Owl 3AP-Cl

by Diros Technology, Inc.

Owl 3AP-Cl is a Class II device made by Diros Technology, Inc., listed in FDA GUDID since 1 Sep 2016 (UDI-DI 00825114005877), 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	Number00825114005877 UDI-DI	Date1 Sep 2016Listed	StatusListed GUDID: in commercial distribution

Official records

AccessGUDID record UDI-DI 00825114005877

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name: Owl
Generic name: Electrical-only medical device connection cable, reusable
Model / Ref / Catalog: 3AP-CL

Primary DI / UDI-DI: 00825114005877
FDA product code: IKD
GMDN term: Electrical-only medical device connection cable, reusable

Device class: Class II
Regulation number: 890.1175
GUDID distribution status: In Commercial Distribution

Sterilisation method: Moist Heat or Steam Sterilization

Similar devices in this category

Other devices filed under Electrical-only medical device connection cable, reusable.

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Properties

Sterilise before use
Prescription use
Premarket exempt
Lot / batch number

Other properties (11, all answered No)