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ArrowPhix System EXARR902526

by Exsomed Corporation

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 NumberB487EXARR9025260 UDI-DIDate6 Apr 2018ListedStatusListed 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  • Withdrawn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
ArrowPhix System
Generic Name
Orthopaedic implant driver
Model / Ref / Catalog
EXARR902526
Description
ArrowPhix Compression Screw System The System includes the implant, two guide wires, and one driver.
Primary DI / UDI-DI
B487EXARR9025260
FDA Product Code
HWC, LXH, HXI
GMDN Term
Orthopaedic implant driver
Device Class
Class II
Regulation Number
888.3040, 888.4540
GUDID distribution status
Not in Commercial Distribution
Size
Length — 26 Millimeter
Outer Diameter — 2.5 Millimeter

Other devices from Exsomed Corporation

Properties

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

Other properties (7)

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