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DeRoyal 13981000

by Deroyal Industries, Inc.

DeRoyal 13981000 is a Class I device made by Deroyal Industries, Inc., listed in FDA GUDID since 21 Jul 2021 (UDI-DI 00749756271943), 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 Number00749756271943 UDI-DI Date21 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  • Withdrawn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
Abdominal binder, reusable
Model / Ref / Catalog
13981000
Primary DI / UDI-DI
00749756271943
FDA product code
FSD
GMDN term
Abdominal binder, reusable
Device class
Class I
Regulation number
880.5160
GUDID distribution status
In Commercial Distribution

Related devices

Category: Abdominal binder, reusable

Similar devices in this category

Other devices filed under Abdominal binder, reusable.

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)