TriLift 30020000BK

GUDID 07290016586534

POLLOGEN LTD

Radio-frequency skin surface treatment system Radio-frequency skin surface treatment system Radio-frequency skin surface treatment system Radio-frequency skin surface treatment system Radio-frequency skin surface treatment system Radio-frequency skin surface treatment system Radio-frequency skin surface treatment system Radio-frequency skin surface treatment system Radio-frequency skin surface treatment system Radio-frequency skin surface treatment system Radio-frequency skin surface treatment system Radio-frequency skin surface treatment system Radio-frequency skin surface treatment system Radio-frequency skin surface treatment system Radio-frequency skin surface treatment system Radio-frequency skin surface treatment system Radio-frequency skin surface treatment system applicator Radio-frequency skin surface treatment system applicator Radio-frequency skin surface treatment system applicator Radio-frequency skin surface treatment system applicator Radio-frequency skin surface treatment system applicator Radio-frequency skin surface treatment system applicator Radio-frequency skin surface treatment system applicator Radio-frequency skin surface treatment system applicator Radio-frequency skin surface treatment system applicator Radio-frequency skin surface treatment system applicator Radio-frequency skin surface treatment system applicator Radio-frequency skin surface treatment system applicator Radio-frequency skin surface treatment system applicator Radio-frequency skin surface treatment system applicator Radio-frequency skin surface treatment system applicator Radio-frequency skin surface treatment system applicator Radio-frequency skin surface treatment system applicator Radio-frequency skin surface treatment system applicator

• Primary Device ID: 07290016586534
• NIH Device Record Key: 5b07004a-c3ea-4b01-a4f0-7e5e2a3cdb39
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: TriLift
• Version Model Number: TriLift
• Catalog Number: 30020000BK
• Company DUNS: 514905681
• Company Name: POLLOGEN LTD
• Device Count: 1
• DM Exempt: true
• Pre-market Exempt: false
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: false
• Serial Number: true
• Manufacturing Date: true
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	07290016586534 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K173503

FDA Product Code

• NGX: Stimulator, Muscle, Powered, For Muscle Conditioning

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2022-02-21
• Device Publish Date: 2022-02-13

Devices Manufactured by POLLOGEN LTD

• 07290016586459 - Desire model U: 2023-12-25 TRIPOLLAR DESIRE PACKED ROSE GOLD USA
• 07290016586626 - STOP VX2 MODEL U: 2023-12-22
• 17290016586487 - triFX: 2022-06-07 H7X7 DISPOSABLE TIP ASSY 5 PACKED BK
• 07290016586497 - triFX: 2022-06-07 GEN100 DISPOSABLE TIP ASSY 5 PACKED BK
• 07290016586503 - triFX: 2022-06-07 GEN 36L DISPOSABLE TIP ASSY 5 PACKED BK
• 07290016586510 - triFX: 2022-06-07 GEN 36 DISPOSABLE TIP ASSY 5 PACKED BK
• 07290016586527 - triFX: 2022-06-07 GEN 12 DISPOSABLE TIP ASSY 5 PACKED BK
• 07290016586534 - TriLift: 2022-02-21
• 07290016586534 - TriLift: 2022-02-21