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Compliance EndoKit™ CEK-1746

by Boston Scientific

Compliance EndoKit™ CEK-1746 is a Class I device made by Boston Scientific, listed in FDA GUDID since 14 Sep 2022 (UDI-DI 00191506034535), 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 Number00191506034535 UDI-DI Date14 Sep 2022ListedStatusListed 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  • Withdrawn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
Compliance EndoKit™
Generic name
Endoscopy preparation kit
Model / Ref / Catalog
CEK-1746
Primary DI / UDI-DI
00191506034535
FDA product code
MNL
GMDN term
Endoscopy preparation kit
Device class
Class I
Regulation number
876.1500
GUDID distribution status
In Commercial Distribution

Related devices

Category: Endoscopy preparation kit

Other devices from Boston Scientific

See all devices from Boston Scientific →

Properties

  • Single use
  • Prescription use
  • Convenience kit
  • Premarket exempt
  • Lot / batch number
Other properties (10, all answered No)