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SUDOSCAN Hand electrode

by Impeto Medical 2 variants

SUDOSCAN Hand electrode (DSPHD) is a Class II device made by Impeto Medical, listed in FDA GUDID since 1 Aug 2022 (UDI-DI 03770025753010), registry data as of 23 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 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number03770025753010 UDI-DI Date1 Aug 2022ListedStatusListed 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  • Withdrawn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
Sudoscan
Generic name
Skin electrical conductance meter
Model / Ref / Catalog
Hand electrode, DSPHD
Primary DI / UDI-DI
03770025753010
FDA product code
GZO
GMDN term
Skin electrical conductance meter
Device class
Class II
Regulation number
882.1540
GUDID distribution status
In Commercial Distribution

Related devices

Category: Skin electrical conductance meter

Similar devices

Other devices filed under FDA product code GZO (Device, Galvanic Skin Response Measurement).

Other devices from Impeto Medical

See all devices from Impeto Medical →

Properties

  • Serial number
  • Manufacturing date
Other properties (13, all answered No)