DEVICE: YUWELL Electronic Blood Pressure Monitor (06933257921634)
Device Identifier (DI) Information
YUWELL Electronic Blood Pressure Monitor
YE8800AR
In Commercial Distribution
JIANGSU YUYUE MEDICAL EQUIPMENT & SUPPLY CO., LTD.
YE8800AR
In Commercial Distribution
JIANGSU YUYUE MEDICAL EQUIPMENT & SUPPLY CO., LTD.
YE8800AR is a rechargeable lithium battery-powered, automatic, noninvasive, wrist-worn blood pressure measuring system intended for over-the-counter (OTC) use. YE8800AR is designed for wrist circumference ranging from 13.5 cm to 19.5 cm. The systolic and diastolic blood pressures are measured using the oscillometric method, where the cuff is inflated with an air pump and deflates via an exhaust valve. During inflation, the cuff pressure is monitored, and pulse waveform data is extracted. The extracted pulse waveform data is then further analyzed by software which determines pulse rate, as well as systolic and diastolic blood pressure.
Device Characteristics
MR Unsafe | |
No | |
No | |
No | |
No | |
Yes | |
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No | |
No |
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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45617 | Automatic-inflation electronic sphygmomanometer, portable, arm/wrist |
An electrically-powered device designed to noninvasively measure blood pressure using a self-contained software program that regulates automatic arm/wrist-cuff inflation and measurement cycles. It typically displays current heart rate and mean arterial pressure in addition to systolic and diastolic blood pressures; it may have memory to store blood pressure values and may sound an alarm if blood pressure exceeds pre-set limits. This device is designed to be portable (e.g., hand-held or carried in a pouch) and is often used for emergency services or home blood pressure monitoring.
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Active | false |
FDA Product Code
[?]Product Code | Product Code Name |
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DXN | System, Measurement, Blood-Pressure, Non-Invasive |
FDA Premarket Submission
FDA Premarket Submission Number [?] | Supplement Number [?] |
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K221372 | 000 |
Sterilization
Storage and Handling
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No storage/handling found |
Clinically Relevant Size
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No Device Sizes |
Device Record Status
bb318c54-b926-4a2d-bd9c-d8800b91da07
June 20, 2025
1
June 12, 2025
June 20, 2025
1
June 12, 2025
Alternative and Additional Identifiers Additional Identifiers
Package DI
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Secondary DI
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Unit of Use DI
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CLOSE
Direct Marking (DM)
[?]Production Identifier(s) in UDI
[?]Customer Contact
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No Customer Contact currently defined