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IV Plus N0830

by Nexus Medical, LLC

IV Plus N0830 is a Class II device made by Nexus Medical, LLC, listed in FDA GUDID since 4 Sep 2024 (UDI-DI 10815879021707), 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 Number10815879021707 UDI-DI Date4 Sep 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  • Withdrawn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

Trade name
IV Plus
Generic name
Stopcock
Model / reference
N0830
Primary DI / UDI-DI
10815879021707
FDA product code
DTL
GMDN term
Stopcock
Device class
Class II
Regulation number
870.4290
GUDID distribution status
In Commercial Distribution

Related devices

Category: Stopcock

Similar devices in this category

Other devices filed under Stopcock.

Other devices from Nexus Medical, LLC

See all devices from Nexus Medical, LLC →

Properties

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