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Bag Decanter 9002

by Remington Medical, Inc.

Bag Decanter 9002 is an intravenous fluid bag spike (FDA Class II; FDA product code LHI, Set, i.V. Fluid transfer) made by Remington Medical, Inc., listed in FDA GUDID since 21 Sep 2016 (UDI-DI 00813079020059), registry data as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00813079020059 UDI-DI Date21 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  • Withdrawn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
Bag Decanter
Generic name
Intravenous fluid bag spike
Model / Ref / Catalog
9002
Primary DI / UDI-DI
00813079020059
FDA product code
LHI
GMDN term
Intravenous fluid bag spike
Device class
Class II
Regulation number
880.5440
GUDID distribution status
In Commercial Distribution
Sterilisation method
Ethylene Oxide
Size
Angle — 35 degree

Related devices

Category: Intravenous fluid bag spike

Similar devices

Other devices filed under FDA product code LHI (Set, i.V. Fluid transfer).

Other devices from Remington Medical, Inc.

See all devices from Remington Medical, Inc. →

Properties

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