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Q-Sense CPM Thermal Sensory Analazer
FDA UDIClass I (US FDA UDI)
by Medoc Corp.
Identity
- Trade Name
- Q-Sense CPM Thermal Sensory Analazer FDA UDI
- Generic Name
- Thermotester, diagnostic FDA UDI
- Device Name
- The Q-Sense CPM Thermal Sensory Analyzer is a QST (Quantitative Sensory Testing) device including advanced software package designed for clinical use and advance research in the field of Pain Management. The CPM Model offers additional capabilities to the Q-Sense device including: Simultaneous operation of two Thermodes, Ramp & Hold method, Computerized Visual Analog Scale (CoVAS). The Device includes: main unit, two thermodes and accessories. FDA UDI
- Model / Reference
- Q-Sense CPM FDA UDI
- Description
- The Q-Sense CPM Thermal Sensory Analyzer is a QST (Quantitative Sensory Testing) device including advanced software package designed for clinical use and advance research in the field of Pain Management. The CPM Model offers additional capabilities to the Q-Sense device including: Simultaneous operation of two Thermodes, Ramp & Hold method, Computerized Visual Analog Scale (CoVAS). The Device includes: main unit, two thermodes and accessories. FDA UDI
Identifiers
- Catalog Number
- MO 00013-CPM FDA UDI
- Primary DI / UDI-DI
- 07290103039257 FDA UDI
- 510(k) Number
- K922052 FDA UDI
- FDA Product Code
- LQW FDA UDI
- GMDN Term
- Thermotester, diagnostic FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 882.1200 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
Yes
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: Thermotester, diagnostic
Q-Sense CPM Thermal Sensory Analazer 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
- Contact Heat Evoked Potential Stimulator — 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
Cleared under the same submission
K922052 also covers:
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 |
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Manufacturer
- Manufacturer
- Medoc Corp.
Sources (1)
- FDA UDI 259ff125-a5ba-4143-b16c-5cb338db11c3 36 fields · synced Jun 8, 2026