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BG 323 Pump System 100-517PXS

by Cme America LLC

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 NumberB101100517PXS0 UDI-DI Date15 Sep 2016ListedStatusListed 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  • Withdrawn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
BG 323 Pump System
Generic Name
Bedside infusion pump, single-channel
Model / Reference
100-517PXS
Primary DI / UDI-DI
B101100517PXS0
FDA Product Code
FRN, MEA
GMDN Term
Bedside infusion pump, single-channel
Device Class
Class II
Regulation Number
880.5725
GUDID distribution status
Not in Commercial Distribution
MRI Safety
MR Unsafe

Properties

  • Prescription Use
  • Convenience Kit
  • Serial Number
  • Manufacturing Date

Other properties (10)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Lot / Batch Number: No
  • Expiration Date: No