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Rivus

by Neurosoft, Ooo 2 variants

Rivus is a Class II device made by Neurosoft, Ooo, listed in FDA GUDID since 20 Dec 2024 (UDI-DI 04650075336922), 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 Number04650075336922 UDI-DI Date20 Dec 2024ListedStatusListed 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  • Withdrawn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

Generic name
Urodynamic measurement system
Model / reference
Rivus
Primary DI / UDI-DI
04650075336922
FDA product code
EXY
GMDN term
Urodynamic measurement system
Device class
Class II
Regulation number
876.1800
GUDID distribution status
In Commercial Distribution

Related devices

Category: Urodynamic measurement system

Similar devices in this category

Other devices filed under Urodynamic measurement system.

Other devices from Neurosoft, Ooo

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Properties

  • Prescription use
  • Premarket exempt
  • Serial number
  • Manufacturing date
Other properties (11, all answered No)