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DeRoyal 32-1308

by Deroyal Industries, Inc.

DeRoyal 32-1308 is a Class I device made by Deroyal Industries, Inc., listed in FDA GUDID since 30 Jun 2021 (UDI-DI 00749756058094), 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 Number00749756058094 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  • Withdrawn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
Rigid endoscopic tissue manipulation forceps, single-use
Model / Ref / Catalog
32-1308
Primary DI / UDI-DI
00749756058094
FDA product code
GEN
GMDN term
Rigid endoscopic tissue manipulation forceps, single-use
Device class
Class I
Regulation number
878.4800
GUDID distribution status
In Commercial Distribution

Related devices

Category: Rigid endoscopic tissue manipulation forceps, single-use

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)