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Alaris, SmartSite 42404E-07

by BD Switzerland Sàrl

Listed FDA GUDID listing, not in commercial distribution

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

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number10885403237904 UDI-DI Date27 Jul 2017ListedStatusListed GUDID: not in commercial distribution

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name
Alaris, SmartSite
Generic Name
Electric infusion pump administration set, single-use
Model / Ref / Catalog
42404E-07
Primary DI / UDI-DI
10885403237904
FDA Product Code
FPA
GMDN Term
Electric infusion pump administration set, single-use
Device Class
Class II
Regulation Number
880.5440
GUDID distribution status
Not in Commercial Distribution

Other devices from BD Switzerland Sàrl

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Properties

  • Sterile
  • Single Use
  • Prescription Use
  • Lot / Batch Number
  • Expiration Date

Other properties (9)

  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No
  • Manufacturing Date: No