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Compliance EndoKit™ CEK-907

by Boston Scientific

Compliance EndoKit™ CEK-907 is a Class I device made by Boston Scientific, listed in FDA GUDID since 5 Nov 2018 (UDI-DI 00840253118493), 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 Number00840253118493 UDI-DI Date5 Nov 2018ListedStatusListed 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  • Withdrawn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-907
Primary DI / UDI-DI
00840253118493
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 kitEndoscope cleaning kit

Similar devices

Other devices filed under FDA product code MNL (ACCESSORIES, CLEANING BRUSHES, FOR ENDOSCOPE).

Other devices from Boston Scientific

See all devices from Boston Scientific →

Properties

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