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DeRoyal SY-0831

by Deroyal Industries, Inc.

DeRoyal SY-0831 is a Class II device made by Deroyal Industries, Inc., listed in FDA GUDID since 10 Mar 2023 (UDI-DI 00749756390163), 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 Number00749756390163 UDI-DI Date10 Mar 2023ListedStatusListed 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  • Withdrawn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
Angiographic syringe
Model / Ref / Catalog
SY-0831
Primary DI / UDI-DI
00749756390163
FDA product code
DXT
GMDN term
Angiographic syringe
Device class
Class II
Regulation number
870.1650
GUDID distribution status
In Commercial Distribution

Related devices

Category: Angiographic syringe

Similar devices in this category

Other devices filed under Angiographic syringe.

Other devices from Deroyal Industries, Inc.

See all devices from Deroyal Industries, Inc. →

Properties

  • Single use
  • Prescription use
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (10, all answered No)