DEVICE: PHYSIO LOGIC DIGIPRO+ DIGITAL THERMOMETER, RECTAL (Red) (00057565166191)
Device Identifier (DI) Information
PHYSIO LOGIC DIGIPRO+ DIGITAL THERMOMETER, RECTAL (Red)
016-619
In Commercial Distribution
016-619
A.M.G. Médicale Inc
016-619
In Commercial Distribution
016-619
A.M.G. Médicale Inc
DigiPro+ ™ single-patient digital thermometers can help to prevent the risk of cross-contamination, nosocomial infections and make it easy to prevent the spread of contamination among patients. What’s more, DigiPro+™ utilizes a “real measurement” technology, which permits read after the beep if a higher temperature is later detected.
Accurate within ± 0.1°C in the 35.5°C to 42°C range
Displays in Celsius or Fahrenheit
Response time: 30 seconds for oral readings
Auto shut-off feature
Memory recall / display of last reading
Individually packaged, includes storage case
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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K163518 | 000 |
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
7f5428ba-3557-4170-a732-56c624e5c47d
June 19, 2023
1
June 09, 2023
June 19, 2023
1
June 09, 2023
Alternative and Additional Identifiers Additional Identifiers
Package DI
[?]Package DI Number | Quantity per Package | Contains DI Package | Package Discontinue Date | Package Status | Package Type |
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00057565975120 | 50 | 00057565166191 | In Commercial Distribution | ||
00057565975137 | 10 | 00057565975120 | In Commercial Distribution |
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
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No Customer Contact currently defined