Skip to content

Olympus MAJ-2223

by KeyMed (Medical and Industrial Equipment) Ltd

Olympus MAJ-2223 (K10037164) is a Class II device made by KeyMed (Medical and Industrial Equipment) Ltd, listed in FDA GUDID since 18 Jul 2023 (UDI-DI 15019778008547), 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 Number15019778008547 UDI-DI Date18 Jul 2023ListedStatusListed 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  • Withdrawn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
Olympus
Generic name
Endoscopic insufflation tubing set, single-use
Model / Ref / Catalog
MAJ-2223, K10037164
Primary DI / UDI-DI
15019778008547
FDA product code
OCX
GMDN term
Endoscopic insufflation tubing set, single-use
Device class
Class II
Regulation number
876.1500
GUDID distribution status
In Commercial Distribution

Related devices

Category: Endoscopic insufflation tubing set, single-use

Similar devices in this category

Other devices filed under Endoscopic insufflation tubing set, single-use.

Other devices from KeyMed (Medical and Industrial Equipment) Ltd

See all devices from KeyMed (Medical and Industrial Equipment) Ltd →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (9, all answered No)