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Sudoscan

FDA UDI

Class II (US FDA UDI)

by Impeto Medical

Identity

Trade Name
SUDOSCAN FDA UDI
Generic Name
Skin electrical conductance meter FDA UDI
Model / Reference
Dock feet FDA UDI

Identifiers

Catalog Number
DSPFD FDA UDI
Primary DI / UDI-DI
03770025753072 FDA UDI
FDA Product Code
GZO FDA UDI
GMDN Term
Skin electrical conductance meter FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.1540 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Skin electrical conductance meter

Sudoscan by Impeto Medical — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Skin electrical conductance meter.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Impeto Medical

Sources (1)

  • FDA UDI e68b4bc2-8e70-44a5-9280-0ebce218a955 34 fields · synced May 30, 2026