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
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
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Manufacturer
- Manufacturer
- Titronics Research & Development Co.
Sources (1)
- FDA UDI 3650e39c-ffc5-4372-8c5e-b62bc1fc36cd 36 fields · synced May 31, 2026