DEVICE: PURELIFT (00860008851024)
Device Identifier (DI) Information
PURELIFT
FACE
In Commercial Distribution
PURELIFT FACE
Xtreem Pulse LLC
FACE
In Commercial Distribution
PURELIFT FACE
Xtreem Pulse LLC
The PureLift Face device is a hand-held device intended to apply electrical impulses to strategic locations on the face. The probes are designed for optimal contact with the face. The device continually alternates between the positive and negative probes and allows the user to adjust the settings for personalized comfort level by pressing the up/down button. The intensity starts at (1) and continues to (10). The device, powered by a 3.7-volt battery, produces low-level current that is transmitted through the two fixed, smooth spherical probes. To turn the device on, the power button is pushed. Then the green LED light will illuminate indicating the unit is ready for use. The two probes gently glide over the skin to deliver low-level electrical impulses to strategic locations on the face with the use of conductive gel. The unit contains a power supply and rechargeable battery. The enclosure is made of medical grade biocompatible plastics and the output contacts (Probes) consist of chrome-plated spheres.
Device Characteristics
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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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66566 | Facial muscle cosmesis electrical stimulator |
An electrically-powered, hand-held device intended to be used in the home to apply electrical stimuli to the facial muscles through the skin (transcutaneously), to improve muscle tone and help tighten overlying skin for cosmetic facial rejuvenation. It includes electrodes at the distal end and controls to adjust the electrical impulse intensity; it is typically used with a gel, which may be supplied with the device, intended to facilitate conduction of the electrical current. This is a reusable device.
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FDA Product Code
[?]Product Code | Product Code Name |
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NFO | Stimulator, Transcutaneous Electrical, Aesthetic Purposes |
FDA Premarket Submission
FDA Premarket Submission Number [?] | Supplement Number [?] |
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K190269 | 000 |
Sterilization
Storage and Handling
[?]Storage and Handling |
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Handling Environment Temperature: between 10 and 45 Degrees Celsius |
Handling Environment Humidity: between 10 and 95 Percent (%) Relative Humidity |
Handling Environment Atmospheric Pressure: between 700 and 1060 KiloPascal |
Clinically Relevant Size
[?]Size Type Text |
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Height: 1.4 Inch |
Width: 4.8 Inch |
Outer Diameter: 4.3 Inch |
Device Record Status
697da0b7-4fa3-4f0e-b9d4-1db903074002
October 09, 2023
1
September 30, 2023
October 09, 2023
1
September 30, 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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No Package DIs found |
Secondary DI
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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