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Renegade™ HI-FLO™ FATHOM™ Kit M001184600

by Boston Scientific GUDID

Listed FDA GUDID listing, not in commercial distribution

Regulatory status

as of 29 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number08714729786207 UDI-DIDate24 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  • Withdrawn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

Recalls

0 recalls · FDA

No FDA recalls on record, checked 23 Oct 2026.

Specification

GUDID

Trade Name
Renegade™ HI-FLO™ FATHOM™ Kit
Generic Name
Vascular microcatheter
Model / Reference
M001184600
Primary DI / UDI-DI
08714729786207
FDA Product Code
KRA
GMDN Term
Vascular microcatheter
Device Class
Class II
Regulation Number
870.1210
GUDID distribution status
Not in Commercial Distribution

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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