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Royal Flush OBRF3-3/4-14

by Royal Knit, Inc.

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

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing NumberG296OBRF334140 UDI-DI Date19 Sep 2022ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
Royal Flush
Generic name
Stump sock
Model / Ref / Catalog
OBRF3-3/4-14
Primary DI / UDI-DI
G296OBRF334140
FDA product code
FQL
GMDN term
Stump sock
Device class
Class I
Regulation number
880.5780
GUDID distribution status
In Commercial Distribution

Related devices

Category: Stump sock

Other devices from Royal Knit, Inc.

See all devices from Royal Knit, Inc. →

Properties

  • Single use
  • Over-the-counter
  • Premarket exempt
  • Lot / batch number

Other properties (11)

  • Supplied sterile: No
  • Sterilise before use: No
  • Implantable: No
  • Contains latex: No
  • Prescription use: No
  • Convenience kit: No
  • Combination product: No
  • HCT/P: No
  • Serial number: No
  • Expiration date: No
  • Manufacturing date: No