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Hospira 465348

by ICU Medical, Inc.

Hospira 465348 (0465348) is a Class II device made by ICU Medical, Inc., listed in FDA GUDID since 1 Sep 2016 (UDI-DI 10887787006640), 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 Number10887787006640 UDI-DI Date1 Sep 2016ListedStatusListed 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  • Withdrawn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
Hospira
Generic name
Venous butterfly needle/set
Model / Ref / Catalog
465348, 0465348
Primary DI / UDI-DI
10887787006640
FDA product code
JOL
GMDN term
Venous butterfly needle/set
Device class
Class II
Regulation number
880.6740
GUDID distribution status
In Commercial Distribution
Size
Length — 30 Inch

Similar devices

Other devices filed under FDA product code JOL (CATHETER AND TIP, SUCTION).

Other devices from ICU Medical, Inc.

See all devices from ICU Medical, Inc. →

Properties

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