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DeRoyal 89-8990

by Deroyal Industries, Inc.

DeRoyal 89-8990 is a Class II device made by Deroyal Industries, Inc., listed in FDA GUDID since 12 Sep 2016 (UDI-DI 00749756894029), 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 Number00749756894029 UDI-DI Date12 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  • Withdrawn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
DeRoyal
Generic name
Epidural anaesthesia set, non-medicated
Model / reference
89-8990
Primary DI / UDI-DI
00749756894029
FDA product code
LRO
GMDN term
Epidural anaesthesia set, non-medicated
Device class
Class II
Regulation number
878.4370
GUDID distribution status
In Commercial Distribution

Related devices

Category: Epidural anaesthesia set, non-medicated

Similar devices

Other devices filed under FDA product code LRO (General surgery tray).

Other devices from Deroyal Industries, Inc.

See all devices from Deroyal Industries, Inc. →

Properties

  • Supplied sterile
  • Single use
  • Convenience kit
  • Lot / batch number
  • Expiration date
Other properties (10, all answered No)