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Trigno Trigger Adapter SP-W01N

by Delsys, Inc.

Trigno Trigger Adapter SP-W01N is a Class II device made by Delsys, Inc., listed in FDA GUDID since 22 Feb 2017 (UDI-DI 00851679007087), registry data as of 22 Oct 2026.

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

Source GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00851679007087 UDI-DI Date22 Feb 2017ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
Trigno Trigger Adapter
Generic name
Biofeedback system
Model / reference
SP-W01N
Primary DI / UDI-DI
00851679007087
FDA product code
HCC
GMDN term
Biofeedback system
Device class
Class II
Regulation number
882.5050
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code HCC (Device, Biofeedback).

Other devices from Delsys, Inc.

See all devices from Delsys, Inc. →

Properties

  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Serial number
Other properties (11, all answered No)