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DeRoyal 32-073

by Deroyal Industries, Inc.

DeRoyal 32-073 is a Class I device made by Deroyal Industries, Inc., listed in FDA GUDID since 30 Jun 2021 (UDI-DI 00749756029124), 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 Number00749756029124 UDI-DI Date30 Jun 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  • Withdrawn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
General-purpose surgical sponge
Model / Ref / Catalog
32-073
Primary DI / UDI-DI
00749756029124
FDA product code
FRL
GMDN term
General-purpose surgical sponge
Device class
Class I
Regulation number
880.5300
GUDID distribution status
In Commercial Distribution

Related devices

Category: General-purpose surgical sponge

Similar devices

Other devices filed under FDA product code FRL (FIBER, MEDICAL, ABSORBENT).

Other devices from Deroyal Industries, Inc.

See all devices from Deroyal Industries, Inc. →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (9, all answered No)