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ClearGuard HD CGHD

by Pursuit Vascular, Inc. GUDID

Listed FDA GUDID listing, not in commercial distribution

Regulatory status

as of 28 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing NumberB081CGHD109193717 UDI-DIDate10 Jan 2017ListedStatusListed GUDID: not 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  • Withdrawn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
ClearGuard HD
Generic Name
Double-lumen haemodialysis catheter, implantable
Model / Reference
CGHD
Primary DI / UDI-DI
B081CGHD109193717
FDA Product Code
PEH
GMDN Term
Double-lumen haemodialysis catheter, implantable
Device Class
Class II
Regulation Number
876.5540
GUDID distribution status
Not in Commercial Distribution

Other devices from Pursuit Vascular, Inc.

Properties

  • Sterile
  • Single Use
  • Implantable
  • Prescription Use
  • Combination Product
  • Premarket Exempt
  • Lot / Batch Number
  • Expiration Date

Other properties (6)

  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • HCT/P: No
  • Serial Number: No
  • Manufacturing Date: No