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BD Alaris™ Infusion Adapter, Software Not Applicable

by CareFusion 303, INC

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 Number10885403510472 UDI-DI Date12 Aug 2022ListedStatusListed 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  • Withdrawn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
BD Alaris™ Infusion Adapter, Software
Generic Name
Infusion pump medication-dosage application software
Model / Ref / Catalog
Not Applicable, INFADPTSW172
Primary DI / UDI-DI
10885403510472
FDA Product Code
PHC
GMDN Term
Infusion pump medication-dosage application software
Device Class
Class II
Regulation Number
880.5725
GUDID distribution status
In Commercial Distribution

Other devices from CareFusion 303, INC

See all devices from CareFusion 303, INC →

Properties

  • Prescription Use
  • Lot / Batch Number

Other properties (12)

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