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ClearGuard HD CGHD

by Pursuit Vascular, Inc. 933 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 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing NumberB081CGHD107204111 UDI-DIDate31 Jul 2017ListedStatusListed 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  • Withdrawn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

Trade Name
ClearGuard HD
Generic Name
Double-lumen haemodialysis catheter, implantable
Model / Reference
CGHD
Primary DI / UDI-DI
B081CGHD107204111
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