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ClariVein® IC 65-018-E4S

by Vascular Insights, LLC

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 Number10854339004027 UDI-DI Date19 Sep 2016ListedStatusListed 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  • Withdrawn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
ClariVein® IC
Generic Name
Peripheral vascular intervention infusion catheter
Model / Ref / Catalog
65-018-E4S
Primary DI / UDI-DI
10854339004027
FDA Product Code
KRA
GMDN Term
Peripheral vascular intervention infusion catheter
Device Class
Class II
Regulation Number
870.1210
GUDID distribution status
Not in Commercial Distribution
Size
Length — 65 Centimeter
Outer Diameter — 0.0345 Inch

Other devices from Vascular Insights, LLC

Properties

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

Other properties (8)

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