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BD Alaris 8110

by CareFusion 303, INC GUDID

Listed FDA GUDID listing, not in commercial distribution

Regulatory status

as of 29 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number10885403517938 UDI-DIDate20 Nov 2023ListedStatusListed GUDID: not in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Recalls

0 recalls · FDA

No FDA recalls on record, checked 23 Oct 2026.

Specification

GUDID

Trade Name
BD Alaris
Generic Name
Bedside syringe pump
Model / Reference
8110
Primary DI / UDI-DI
10885403517938
FDA Product Code
FRN
GMDN Term
Bedside syringe pump
Device Class
Class II
Regulation Number
880.5725
GUDID distribution status
Not in Commercial Distribution
MRI Safety
MR Unsafe

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Properties

  • Prescription Use
  • Serial 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
  • Lot / Batch Number: No
  • Expiration Date: No
  • Manufacturing Date: No