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N/A 50-7280A

by Carefusion 2200, Inc GUDID

Listed FDA GUDID listing, no authorization on record

Regulatory status

as of 29 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number10885403502408 UDI-DIDate9 Mar 2021ListedStatusListed GUDID: 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  • Withdrawn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

Generic Name
Pleural catheter syringe-infusion set
Model / Ref / Catalog
50-7280A
Primary DI / UDI-DI
10885403502408
FDA Product Code
DWM, PNG
GMDN Term
Pleural catheter syringe-infusion set
Device Class
Class II
Regulation Number
870.5050, 876.5630
GUDID distribution status
In Commercial Distribution

Related devices

Category: Pleural catheter syringe-infusion set

Other devices from Carefusion 2200, Inc.

See all devices from Carefusion 2200, Inc. →

Properties

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

Other properties (8)

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