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BD Alaris Pump Infusion Set 388366

by BD Switzerland Sàrl

BD Alaris Pump Infusion Set 388366 is a Class II device made by BD Switzerland Sàrl, listed in FDA GUDID since 23 Oct 2026 (UDI-DI 10885403533822), registry data as of 9 Nov 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 9 Nov 2026.

Regulatory status

as of registry sync 9 Nov 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number10885403533822 UDI-DI Date23 Oct 2026ListedStatusListed 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  • Withdrawn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
BD Alaris Pump Infusion Set
Generic name
Electric infusion pump administration set, single-use
Model / Ref / Catalog
388366
Primary DI / UDI-DI
10885403533822
FDA product code
FPA
GMDN term
Electric infusion pump administration set, single-use
Device class
Class II
Regulation number
880.5440
GUDID distribution status
In Commercial Distribution
MRI safety
MR Safe
Size
Length — 320 Centimeter

Other devices from BD Switzerland Sàrl

See all devices from BD Switzerland Sàrl →

Properties

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