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Lifeshield 1932448

by ICU Medical, Inc.

Lifeshield 1932448 is a Class II device made by ICU Medical, Inc., listed in FDA GUDID since 1 Sep 2016 (UDI-DI 10887787007630), 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 Number10887787007630 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  • Withdrawn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
Lifeshield
Generic name
Venous butterfly needle/set
Model / Ref / Catalog
1932448
Primary DI / UDI-DI
10887787007630
FDA product code
FPA
GMDN term
Venous butterfly needle/set
Device class
Class II
Regulation number
880.5440
GUDID distribution status
In Commercial Distribution
Size
Length — 111 Inch

Similar devices

Other devices filed under FDA product code FPA (Set, administration, intravascular).

Other devices from ICU Medical, Inc.

See all devices from ICU Medical, Inc. →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Lot / batch number
  • Expiration date
Other properties (10, all answered No)