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Custom Procedure Kit 4002888

by Medivators Inc.

Custom Procedure Kit 4002888 is a Class II device made by Medivators Inc., listed in FDA GUDID since 18 Dec 2020 (UDI-DI 40677964020443), 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 Number40677964020443 UDI-DI Date18 Dec 2020ListedStatusListed 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  • Withdrawn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
Custom Procedure Kit
Generic name
Endoscopy preparation kit
Model / Ref / Catalog
4002888
Primary DI / UDI-DI
40677964020443
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)