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FLOQSwabs® 53380CS01

by Copan Italia SpA

FLOQSwabs® 53380CS01 is a Class I device made by Copan Italia SpA, listed in FDA GUDID since 20 Mar 2026 (UDI-DI 38053326007027), 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 Number38053326007027 UDI-DI Date20 Mar 2026ListedStatusListed 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  • Withdrawn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
FLOQSwabs®
Generic name
General-purpose absorbent tip applicator/swab, single-use
Model / Ref / Catalog
53380CS01
Primary DI / UDI-DI
38053326007027
FDA product code
KXG
GMDN term
General-purpose absorbent tip applicator/swab, single-use
Device class
Class I
Regulation number
880.6025
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code KXG (Applicator, Absorbent Tipped, Sterile).

Other devices from Copan Italia SpA

See all devices from Copan Italia SpA →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (9, all answered No)