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Toskani WNE-01

by Toskani Sl.

Listed FDA GUDID listing, no authorization on record

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 Number08436560853152 UDI-DI Date12 Dec 2025ListedStatusListed GUDID: 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  • Withdrawn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
Toskani
Generic Name
Transcutaneous electrical stimulation lead
Model / Ref / Catalog
WNE-01, TKN-00-0315
Primary DI / UDI-DI
08436560853152
FDA Product Code
ISA
GMDN Term
Transcutaneous electrical stimulation lead
Device Class
Class I
Regulation Number
890.5660
GUDID distribution status
In Commercial Distribution
MRI Safety
MR Unsafe

Other devices from Toskani Sl.

Properties

  • Premarket Exempt
  • Lot / Batch Number
  • Serial Number
  • Expiration Date
  • Manufacturing Date

Other properties (9)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Prescription Use: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No