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NovaPort cannula

by Novalung GmbH 4 variants

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 31 May 2026. What this means

Regulatory status

as of registry sync 31 May 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number04260058550735 UDI-DI Date30 Sep 2015ListedStatusListed 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  • Withdrawn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

Generic Name
Cardiopulmonary bypass cannula, femoral
Model / Ref / Catalog
NovaPort® one Vascular Access and Introducer Kit, 8800078
Primary DI / UDI-DI
04260058550735
FDA Product Code
DWF
GMDN Term
Cardiopulmonary bypass cannula, femoral
Device Class
Class II
Regulation Number
870.4210
GUDID distribution status
Not in Commercial Distribution
Size
Catheter Gauge — 15 French

Other devices from Novalung GmbH

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