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Mediplus 2300E

by Mediplus, Ltd.

Mediplus 2300E is a Class II device made by Mediplus, Ltd., listed in FDA GUDID since 16 Sep 2016 (UDI-DI 05055140701107), not in commercial distribution (GUDID) as of 22 Oct 2026.

Listed FDA GUDID listing, not in commercial distribution

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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number05055140701107 UDI-DI Date16 Sep 2016ListedStatusListed GUDID: not 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  • Withdrawn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
Mediplus
Generic name
Gastrointestinal motility manometric catheter, non-electronic
Model / reference
2300E
Primary DI / UDI-DI
05055140701107
FDA product code
KLA
GMDN term
Gastrointestinal motility manometric catheter, non-electronic
Device class
Class II
Regulation number
876.1725
GUDID distribution status
Not in Commercial Distribution
Size
Outer Diameter — 4.5 Millimeter
Length — 150.0 Centimeter

Similar devices

Other devices filed under FDA product code KLA (MONITOR, ESOPHAGEAL MOTILITY, AND TUBE).

Other devices from Mediplus, Ltd.

See all devices from Mediplus, Ltd. →

Properties

  • Single use
  • Prescription use
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (10, all answered No)