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Preclean Kit 4001124

by Medivators Inc.

Preclean Kit 4001124 is a Class II device made by Medivators Inc., listed in FDA GUDID since 21 Jan 2025 (UDI-DI 40677964010642), 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 Number40677964010642 UDI-DI Date21 Jan 2025ListedStatusListed 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  • Withdrawn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
Preclean Kit
Generic name
Endoscopy preparation kit
Model / Ref / Catalog
4001124
Primary DI / UDI-DI
40677964010642
FDA product code
NWU
GMDN term
Endoscopy preparation kit
Device class
Class II
Regulation number
876.1500
GUDID distribution status
In Commercial Distribution

Related devices

Category: Endoscopy preparation kit

Other devices from Medivators Inc.

See all devices from Medivators Inc. →

Properties

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