Identity
- Trade Name
- McKesson FDA UDI
- Generic Name
- Intermittent electronic patient thermometer FDA UDI
- Device Name
- THERMOMETER, ORAL AXILLARY FDA UDI
- Model / Reference
- 3074 FDA UDI
- Description
- THERMOMETER, ORAL AXILLARY FDA UDI
Identifiers
- Primary DI / UDI-DI
- 10612479195841 FDA UDI
- FDA Product Code
- FLL FDA UDI
- GMDN Term
- Intermittent electronic patient thermometer FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 880.2910 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
No
FDA UDI
Over-the-Counter
Yes
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
Category: Intermittent electronic patient thermometer
This continuous measurement thermometer, or oral axillary, is a handheld device designed to measure a patient's body temperature. It features an electronic unit with a attached probe that detects and converts changes in temperature into electrical characteristics, which are then processed and displayed for a short period.
Similar devices
Also classified as Intermittent electronic patient thermometer.
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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
- Mckesson Medical-Surgical Inc.
Sources (1)
- FDA UDI 4d3c6dad-363e-4277-aba7-97fb515fb0ac 33 fields · synced Jun 26, 2026