Skip to content

Kolplast Sol Salina 3ml/2SWAB T10 Est

by Kolplast CI SA

Kolplast Sol Salina 3ml/2SWAB T10 Est (10.4118) is a Class I device made by Kolplast CI SA, listed in FDA GUDID since 29 Nov 2023 (UDI-DI 07898027908682), 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 Number07898027908682 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  • Withdrawn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
Saline suspension medium/diluent IVD
Model / Ref / Catalog
SOL SALINA 3ML/2SWAB T10 EST, 10.4118
Primary DI / UDI-DI
07898027908682
FDA product code
JSG
GMDN term
Saline suspension medium/diluent IVD
Device class
Class I
Regulation number
866.2300
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code JSG (Culture Media, Non-Selective And Non-Differential).

Other devices from Kolplast CI SA

See all devices from Kolplast CI SA →

Properties

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