Dermasculpt

GUDID 10652927775928

CosmoFrance

Tissue injection cannula

• Primary Device ID: 10652927775928
• NIH Device Record Key: e4b1a1de-36c8-486b-9e11-211308a4b2cd
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Dermasculpt
• Version Model Number: DS23G30
• Company DUNS: 015144539
• Company Name: CosmoFrance
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	10652927775928 [Primary]

FDA Product Code

• GEA: Cannula, Surgical, General & Plastic Surgery

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2024-01-31
• Device Publish Date: 2024-01-23

On-Brand Devices [Dermasculpt]

• 10652927785514: DS23G40
• 10652927784845: DS27G40
• 10652927777458: DS25G40
• 10652927775935: DS23G50
• 10652927775928: DS23G30
• 10652927775911: DS22G70
• 10652927729457: DS27G50
• 10652927729440: DS25G50
• 10652927729433: DS18G70
• 10652927727903: DS22G50
• 10652927727644: DS27G38
• 10652927727637: DS27G25
• 10652927727620: DS25G38
• 10652927727569: DS30G25