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DeRoyal 32-2062

by Deroyal Industries, Inc.

DeRoyal 32-2062 is a Class I device made by Deroyal Industries, Inc., listed in FDA GUDID since 3 Mar 2023 (UDI-DI 00749756872034), 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 Number00749756872034 UDI-DI Date3 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  • Withdrawn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
Breathing circuit catheter mount, single-use
Model / Ref / Catalog
32-2062
Primary DI / UDI-DI
00749756872034
FDA product code
BYX
GMDN term
Breathing circuit catheter mount, single-use
Device class
Class I
Regulation number
868.5860
GUDID distribution status
In Commercial Distribution

Related devices

Category: Breathing circuit catheter mount, single-use

Similar devices in this category

Other devices filed under Breathing circuit catheter mount, single-use.

Other devices from Deroyal Industries, Inc.

See all devices from Deroyal Industries, Inc. →

Properties

  • Supplied sterile
  • Single use
  • Contains latex
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (8, all answered No)