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SurfRider 13 Microcatheter N01-13165-ST

by Kaneka Americas Holding, Inc.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

None found

in data synced 22 Oct 2026

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00810201980007 UDI-DI Date17 Feb 2026ListedStatusListed GUDID: in commercial distribution

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 22 Oct 2026.

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade Name
SurfRider 13 Microcatheter
Generic Name
Vascular microcatheter
Model / Reference
N01-13165-ST
Primary DI / UDI-DI
00810201980007
510(k) Number
FDA Product Code
QJP, KRA
GMDN Term
Vascular microcatheter
Device Class
Class II
Regulation Number
870.1250, 870.1210
GUDID distribution status
In Commercial Distribution
Size
Catheter Working Length — 165 Centimeter

Related devices

Cleared under the same submission (K251668)

Other devices from Kaneka Americas Holding, Inc.

Properties

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

Other properties (9)

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