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DeRoyal 54-5010

by Deroyal Industries, Inc.

DeRoyal 54-5010 is a Class I device made by Deroyal Industries, Inc., listed in FDA GUDID since 12 Jul 2021 (UDI-DI 00749756767941), 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 Number00749756767941 UDI-DI Date12 Jul 2021ListedStatusListed 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  • Withdrawn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
DeRoyal
Generic name
Basic intravenous administration set, noninvasive
Model / Ref / Catalog
54-5010
Primary DI / UDI-DI
00749756767941
FDA product code
KYX
GMDN term
Basic intravenous administration set, noninvasive
Device class
Class I
Regulation number
880.6430
GUDID distribution status
In Commercial Distribution

Related devices

Category: Basic intravenous administration set, noninvasive

Other devices from Deroyal Industries, Inc.

See all devices from Deroyal Industries, Inc. →

Properties

  • Single use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (10, all answered No)