Contact Heat Evoked Potential Stimulator

FDA UDI

Class I (US FDA UDI)

by Medoc Corp.

Identity

Trade Name: Contact Heat Evoked Potential Stimulator FDA UDI
Generic Name: Thermotester, diagnostic FDA UDI
Device Name: The Modified Contact Heat Evoked Potential Stimulator (CHEPS) is an advanced, computerized thermal stimulator designed for advanced pain research. This non-invasive device can be used as stimulator for creating sensation and pain stimuli in the sensory nerves fibers. the CHEPS indicated for the use in evaluating the functionality of human reception and transmission of sensory pathways The Device includes: main electrical unit, external cooling unit, at least one thermode probe and accessories. FDA UDI
Model / Reference: CHEPS FDA UDI
Description: The Modified Contact Heat Evoked Potential Stimulator (CHEPS) is an advanced, computerized thermal stimulator designed for advanced pain research. This non-invasive device can be used as stimulator for creating sensation and pain stimuli in the sensory nerves fibers. the CHEPS indicated for the use in evaluating the functionality of human reception and transmission of sensory pathways The Device includes: main electrical unit, external cooling unit, at least one thermode probe and accessories. FDA UDI

Identifiers

Primary DI / UDI-DI: 07290103039318 FDA UDI
FDA Product Code: LQW FDA UDI
NTU FDA UDI
GMDN Term: Thermotester, diagnostic FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 882.1200 FDA UDI
882.1870 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

MRI Safety

MR Conditional FDA UDI

Category: Thermotester, diagnostic

Contact Heat Evoked Potential Stimulator by Medoc Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Thermotester, diagnostic.

NEURO TOUCH — YOSTRA LABS PRIVATE LIMITED · Class I
Thermode 30x30mm (Q-Sense) — Medoc Corp. · Class I
Q-Sense Response Unit — Medoc Corp. · Class I
Thermode 6mm diameter — Medoc Corp. · Class I
Thermode fMRI 16X16mm - including fMRI filter — Medoc Corp. · Class I
Thermode CHEPS fMRI — Medoc Corp. · Class I
Thermode 16X16 (TSA 2) — Medoc Corp. · Class I
Thermode CHEPS — Medoc Corp. · Class I

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer: Medoc Corp.

Sources (1)

FDA UDI 85abe8b1-cd6e-4b46-97d4-82d1e23e56c6 33 fields · synced Jun 1, 2026