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Alaris, SmartSite 10817920

by BD Switzerland Sàrl

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

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 Number10885403234521 UDI-DI Date22 Sep 2016ListedStatusListed GUDID: 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  • Withdrawn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
10817920
Primary DI / UDI-DI
10885403234521
FDA Product Code
FPA, LHI
GMDN Term
Electric infusion pump administration set, single-use
Device Class
Class II
Regulation Number
880.5440
GUDID distribution status
In Commercial Distribution
Size
Length — 123 Inch

Related devices

Category: Electric infusion pump administration set, single-use

Other devices from BD Switzerland Sàrl

See all devices from BD Switzerland Sàrl →

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