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Foot control S-NW3 (Dongle) 30495000

by W&H Dentalwerk Burmoos

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 NumberJ021304950001 UDI-DI Date18 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  • Withdrawn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
Foot control S-NW3 (Dongle)
Generic Name
Foot-switch, electrical
Model / Reference
30495000
Primary DI / UDI-DI
J021304950001
FDA Product Code
EBW, ERL, DZI, HWE, GEY
GMDN Term
Foot-switch, electrical
Device Class
Class I
Regulation Number
872.4200, 874.4250, 872.4120, 878.4820
GUDID distribution status
In Commercial Distribution

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Properties

  • Prescription Use
  • Serial Number
  • Manufacturing Date

Other properties (11)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Lot / Batch Number: No
  • Expiration Date: No