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N/A 50-7290A

by Carefusion 2200, 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 Number10885403502415 UDI-DI Date9 Mar 2021ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Generic Name
Pleural/peritoneal drainage catheterization kit, non-medicated
Model / Ref / Catalog
50-7290A
Primary DI / UDI-DI
10885403502415
FDA Product Code
DWM, PNG
GMDN Term
Pleural/peritoneal drainage catheterization kit, non-medicated
Device Class
Class II
Regulation Number
870.5050, 876.5630
GUDID distribution status
In Commercial Distribution

Related devices

Category: Pleural/peritoneal drainage catheterization kit

Other devices from Carefusion 2200, Inc.

See all devices from Carefusion 2200, Inc. →

Properties

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

Other properties (7)

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