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Mediplus 91255

by Mediplus, Ltd.

Mediplus 91255 is a Class II device made by Mediplus, Ltd., listed in FDA GUDID since 16 Sep 2016 (UDI-DI 05055140702838), 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 Number05055140702838 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  • Withdrawn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
Urological pressure monitoring tubing set
Model / reference
91255
Primary DI / UDI-DI
05055140702838
FDA product code
FEN
GMDN term
Urological pressure monitoring tubing set
Device class
Class II
Regulation number
876.1620
GUDID distribution status
Not in Commercial Distribution
Size
Lumen/Inner Diameter — 1.5 Millimeter
Length — 125.0 Centimeter
Outer Diameter — 3.1 Millimeter

Similar devices

Other devices filed under FDA product code FEN (DEVICE, CYSTOMETRIC, HYDRAULIC).

Other devices from Mediplus, Ltd.

See all devices from Mediplus, Ltd. →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (8, all answered No)