Skip to content

IV Plus® BD6018

by Nexus Medical, LLC

IV Plus® BD6018 is a Class I device made by Nexus Medical, LLC, listed in FDA GUDID since 9 Jun 2017 (UDI-DI 10815879021028), 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 Number10815879021028 UDI-DI Date9 Jun 2017ListedStatusListed 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  • Withdrawn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
Blood collection tube spike syringe adaptor
Model / reference
BD6018
Primary DI / UDI-DI
10815879021028
FDA product code
KST
GMDN term
Blood collection tube spike syringe adaptor
Device class
Class I
Regulation number
864.9125
GUDID distribution status
In Commercial Distribution

Related devices

Category: Blood collection tube spike syringe adaptor

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)