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Titronics

FDA UDI

Class II (US FDA UDI)

by Titronics Research & Development Co.

Identity

Trade Name
Titronics FDA UDI
Generic Name
Thermographic camera FDA UDI
Device Name
The C-5000 is indicated for use in detecting, measuring, recording, and graphing the skin surface temperature on both sides of the spine of adults and children by chiropractors. It is to be used before and after therapy is rendered as part of monitoring the patient's response to care, similar to a common thermometer FDA UDI
Model / Reference
Tytron C-5000 FDA UDI
Description
The C-5000 is indicated for use in detecting, measuring, recording, and graphing the skin surface temperature on both sides of the spine of adults and children by chiropractors. It is to be used before and after therapy is rendered as part of monitoring the patient's response to care, similar to a common thermometer FDA UDI

Identifiers

Primary DI / UDI-DI
00860447001707 FDA UDI
FDA Product Code
HCS FDA UDI
GMDN Term
Thermographic camera FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.1570 FDA UDI
Commercial Distribution
Not 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

No

FDA UDI

Titronics by Titronics Research & Development Co. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 3650e39c-ffc5-4372-8c5e-b62bc1fc36cd 36 fields · synced May 31, 2026