Diamond applicator

GUDID 07290016540314

Diamondpolar applicator is designed for use in dermatological procedures requiring treatment of moderate to severe facial wrinkles and rhytides.

VENUS CONCEPT LTD

Radio-frequency skin contouring system applicator, bipolar Radio-frequency skin contouring system applicator, bipolar Radio-frequency skin contouring system applicator, bipolar Radio-frequency skin contouring system applicator, bipolar Radio-frequency skin contouring system applicator, bipolar Radio-frequency skin contouring system applicator, bipolar Radio-frequency skin contouring system applicator, bipolar Radio-frequency skin contouring system applicator, bipolar Radio-frequency skin contouring system applicator, bipolar Radio-frequency skin contouring system applicator, bipolar Radio-frequency skin contouring system applicator, bipolar Radio-frequency skin contouring system applicator, bipolar Radio-frequency skin contouring system applicator, bipolar Radio-frequency skin contouring system applicator, bipolar Radio-frequency skin contouring system applicator, bipolar Radio-frequency skin contouring system applicator, bipolar Radio-frequency skin contouring system applicator, bipolar

• Primary Device ID: 07290016540314
• NIH Device Record Key: 7a302a01-0966-4e98-8335-851da9d87258
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Diamond applicator
• Version Model Number: AS110009
• Company DUNS: 533127663
• Company Name: VENUS CONCEPT LTD
• Device Count: 1
• DM Exempt: false
• 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: false
• 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	07290016540314 [Primary]
GS1	07290016540369 [Package]; Package: [1 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K150161

FDA Product Code

• GEI: Electrosurgical, Cutting & Coagulation & Accessories

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2016-09-24

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