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DeRoyal 31-588

by Deroyal Industries, Inc.

DeRoyal 31-588 is a Class I device made by Deroyal Industries, Inc., listed in FDA GUDID since 30 Jun 2021 (UDI-DI 00749756029957), 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 Number00749756029957 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  • Withdrawn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
Laparoscopic blunt dissector
Model / Ref / Catalog
31-588
Primary DI / UDI-DI
00749756029957
FDA product code
GDI
GMDN term
Laparoscopic blunt dissector
Device class
Class I
Regulation number
878.4800
GUDID distribution status
In Commercial Distribution

Related devices

Category: Laparoscopic blunt dissector

Similar devices

Other devices filed under FDA product code GDI (DISSECTOR, SURGICAL, GENERAL & PLASTIC SURGERY).

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)