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Kolplast Swab Haste Regular D2, 5 Fp Est

by Kolplast CI SA

Kolplast Swab Haste Regular D2, 5 Fp Est (10.4109) is a Class I device made by Kolplast CI SA, listed in FDA GUDID since 29 Nov 2023 (UDI-DI 07898027905353), 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 Number07898027905353 UDI-DI Date29 Nov 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  • Withdrawn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
Kolplast
Generic name
General-purpose absorbent tip applicator/swab, single-use
Model / Ref / Catalog
SWAB HASTE REGULAR D2, 5 FP EST, 10.4109
Primary DI / UDI-DI
07898027905353
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

Related devices

Category: General-purpose absorbent tip applicator/swab, single-use

Similar devices in this category

Other devices filed under General-purpose absorbent tip applicator/swab, single-use.

Other devices from Kolplast CI SA

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Properties

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