DEVICE: Accuflex5 VU Thermometer, from Physio Logic (00057565166511)
Device Identifier (DI) Information
Accuflex5 VU Thermometer, from Physio Logic
016-651
In Commercial Distribution
016-651
A.M.G. Médicale Inc
016-651
In Commercial Distribution
016-651
A.M.G. Médicale Inc
Accurate readings in as little as 5 seconds.
•Color feverline alert indicates if the reading is normal or if it represents a mild or high fever.
•Large, backlit screen displays temperature in °C or °F.
•Beeps when reading is complete.
•Professional accuracy within 0.1°C (0.2°F).
•Waterproof gentle–flex tip for added comfort & safety.
•Recalls last reading.
•Can be used orally, rectally, under the arm or to take bath water temperature.
•Auto shut-off for extended battery life
Device Characteristics
Labeling does not contain MRI Safety Information | |
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GMDN
[?]GMDN© Term Code, Names and Definitions (*Terms of Use): GMDN® is a registered trademark of The GMDN Agency. All rights reserved. Used under licence from The GMDN Agency Ltd.
GMDN Term Code | GMDN Term Name | GMDN Term Definition | GMDN Term Status [?] | Implantable? |
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14035 | Intermittent electronic patient thermometer |
A hand-held, battery-powered, electronic instrument designed to measure a patient's body temperature. It may comprise an electronic unit with an attached probe or be a single unit (shaped like an ordinary hand-held capillary thermometer) that detects and converts the changes in temperature into variations of some electrical characteristic, e.g., resistance or voltage. These variations of the electrical characteristics are processed in the electronic circuits and in turn displayed, for a short period, as temperature readings. Thereafter the display will automatically turn off or go into standby mode. This is a reusable device.
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Active | false |
FDA Product Code
[?]Product Code | Product Code Name |
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FLL | Thermometer, Electronic, Clinical |
FDA Premarket Submission
FDA Premarket Submission Number [?] | Supplement Number [?] |
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Premarket Submission Number Not Available/Not Released |
Sterilization
Storage and Handling
[?]Storage and Handling |
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No storage/handling found |
Clinically Relevant Size
[?]Size Type Text |
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No Device Sizes |
Device Record Status
382c4279-ec2f-4216-b5f4-09559c9c34f6
August 21, 2020
3
May 16, 2018
August 21, 2020
3
May 16, 2018
Alternative and Additional Identifiers Additional Identifiers
Package DI
[?]Package DI Number | Quantity per Package | Contains DI Package | Package Discontinue Date | Package Status | Package Type |
---|---|---|---|---|---|
05756599923224 | 12 | 05756599922548 | In Commercial Distribution | Case | |
05756599922548 | 6 | 00057565166511 | In Commercial Distribution | Box | |
10057565166518 | 6 | 00057565166511 | In Commercial Distribution | Inner box | |
20057565166515 | 12 | 10057565166518 | In Commercial Distribution | Master case |
Secondary DI
[?]Issuing Agency [?] | Secondary DI Number |
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No Secondary DIs found |
Unit of Use DI
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Unit of Use DI Number:
No Unit of Use DI Numbers Found
CLOSE
Direct Marking (DM)
[?]Production Identifier(s) in UDI
[?]Customer Contact
[?]
No Customer Contact currently defined