Q-Sense Response Unit

FDA UDI

Class I (US FDA UDI)

by Medoc Corp.

Identity

Trade Name: Q-Sense Response Unit FDA UDI
Generic Name: Thermotester, diagnostic FDA UDI
Device Name: Q-Sense PRU (TSA) FDA UDI
Model / Reference: Q-Sense FDA UDI
Description: Q-Sense PRU (TSA) FDA UDI

Identifiers

Catalog Number: AS 00403 FDA UDI
Primary DI / UDI-DI: 07290103039233 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

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

Yes

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Thermotester, diagnostic

Q-Sense Response Unit by Medoc Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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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

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Manufacturer

Manufacturer: Medoc Corp.

Sources (1)

FDA UDI 60c41877-34b9-4b6d-b958-4c9a3e786f72 34 fields · synced May 31, 2026