Skip to content

KT ™ Premium Slides

by Slmp, LLC 7 variants

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 Number04062418017175 UDI-DI Date21 Sep 2026ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Generic Name
General specimen microscopy slide IVD, single-use
Model / Ref / Catalog
KT Slides KT3+ Supa Mega large format adhesive premium slide, 90 degree corners, KT3+-SUPA-90
Primary DI / UDI-DI
04062418017175
FDA Product Code
KEW
GMDN Term
General specimen microscopy slide IVD, single-use
Device Class
Class I
Regulation Number
864.3010
GUDID distribution status
In Commercial Distribution

Other devices from Slmp, LLC

See all devices from Slmp, LLC →

Properties

  • Single Use
  • Premarket Exempt

Other properties (12)

  • Sterile: No
  • Implantable: No
  • Contains Latex: No
  • Prescription Use: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Lot / Batch Number: No
  • Serial Number: No
  • Expiration Date: No
  • Manufacturing Date: No