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Mms MMS5415

by Mediplus, Ltd.

Mms MMS5415 is a Class I device made by Mediplus, Ltd., listed in FDA GUDID since 16 Sep 2016 (UDI-DI 05055140703149), 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 Number05055140703149 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  • Withdrawn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
Mms
Generic name
Urodynamic measurement system
Model / reference
MMS5415
Primary DI / UDI-DI
05055140703149
FDA product code
KGZ
GMDN term
Urodynamic measurement system
Device class
Class I
Regulation number
878.4200
GUDID distribution status
Not in Commercial Distribution
Size
Length — 200.0 Centimeter
Catheter Gauge — 4.5 French

Similar devices

Other devices filed under FDA product code KGZ (ACCESSORIES, CATHETER).

Other devices from Mediplus, Ltd.

See all devices from Mediplus, Ltd. →

Properties

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