Skip to content

Owl 473-001

by Diros Technology, Inc.

Owl 473-001 is a Class II device made by Diros Technology, Inc., listed in FDA GUDID since 1 Sep 2016 (UDI-DI 00825114000384), 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 Number00825114000384 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  • Withdrawn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
Electrical-only medical device connection cable, reusable
Model / Ref / Catalog
473-001
Primary DI / UDI-DI
00825114000384
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

Related devices

Category: Electrical-only medical device connection cable, reusable

Similar devices in this category

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

Other devices from Diros Technology, Inc.

See all devices from Diros Technology, Inc. →

Properties

  • Sterilise before use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
Other properties (11, all answered No)