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Quantum Perfusion Dual Lumen Cannula 24F DL24F-V0

by Spectrum Medical Limited GUDID

Listed FDA GUDID listing, no authorization on record

Regulatory status

as of 29 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number18051160300812 UDI-DIDate21 May 2026ListedStatusListed 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  • Withdrawn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

Trade Name
Quantum Perfusion Dual Lumen Cannula 24F
Generic Name
Cardiopulmonary bypass/extracorporeal membrane oxygenation cannula, drainage
Model / Reference
DL24F-V0
Primary DI / UDI-DI
18051160300812
510(k) Number
FDA Product Code
DWF
GMDN Term
Cardiopulmonary bypass/extracorporeal membrane oxygenation cannula, drainage
Device Class
Class II
Regulation Number
870.4210
GUDID distribution status
In Commercial Distribution
MRI Safety
MR Unsafe

Related devices

Cleared under the same submission (K203067)

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Properties

  • Sterile
  • Single Use
  • Prescription Use
  • Lot / Batch Number
  • Expiration Date
  • Manufacturing Date

Other properties (8)

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