Skip to content

VersaCross RF Wire VXW-35-230-J

by Baylis Médicale Cie Inc

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 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00685447003304 UDI-DI Date1 May 2019ListedStatusListed 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  • Withdrawn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
VersaCross RF Wire
Generic Name
Endoscopic electrosurgical electrode, monopolar, single-use
Model / Reference
VXW-35-230-J
Primary DI / UDI-DI
00685447003304
FDA Product Code
DXF
GMDN Term
Endoscopic electrosurgical electrode, monopolar, single-use
Device Class
Class II
Regulation Number
870.5175
GUDID distribution status
Not in Commercial Distribution

Related devices

Category: Endoscopic electrosurgical electrode, monopolar, single-use

Other devices from Baylis Médicale Cie Inc

See all devices from Baylis Médicale Cie Inc →

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