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NA Venous HLS Cannula, uncoated

by Maquet Cardiopulmonary AG 8 variants

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

None found

in data synced 23 Oct 2026

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 Number04037691774916 UDI-DI Date24 Oct 2015ListedStatusListed GUDID: in commercial distribution

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 23 Oct 2026.

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Generic Name
Peripheral vascular catheter
Model / Ref / Catalog
Venous HLS Cannula, uncoated, 70105.3924
Primary DI / UDI-DI
04037691774916
510(k) Number
FDA Product Code
DWF
GMDN Term
Peripheral vascular catheter
Device Class
Class II
Regulation Number
870.4210
GUDID distribution status
In Commercial Distribution
Size
Catheter Gauge — 25 French

Related devices

Category: Peripheral vascular catheter

Cleared under the same submission (K102532)

Show all (12)

Other devices from Maquet Cardiopulmonary AG

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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