Dermasculpt

GUDID 10652927820789

Demetech Corporation

Tissue injection cannula

• Primary Device ID: 10652927820789
• NIH Device Record Key: 7a6b7910-ec9f-4087-851b-ac0e9f15c5f7
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Dermasculpt
• Version Model Number: DS24G40
• Company DUNS: 039436691
• Company Name: Demetech Corporation
• 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	10652927820789 [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: 2025-08-14
• Device Publish Date: 2025-08-06

Devices Manufactured by Demetech Corporation

• 10652927820789 - Dermasculpt: 2025-08-14
• 10652927820789 - Dermasculpt: 2025-08-14
• 30652927684422 - DemeSILK: 2024-03-22 Nonabsorbable Silk Surgical Suture
• 30652927776882 - DemeDIOX: 2024-03-22 Absorbable Polydioxanone Surgical Suture
• 30652927777513 - DemeSILK: 2024-03-22 Nonabsorbable Silk Surgical Suture
• 30652927777636 - DemeSILK: 2024-03-22 Nonabsorbable Silk Surgical Suture
• 30652927777728 - DemeSILK: 2024-03-22 Nonabsorbable Silk Surgical Suture
• 30652927777827 - DemeSTEEL: 2024-03-22 Stainless Steel Surgical Non Absorbable Suture
• 30652927778114 - DemeDIOX: 2024-03-22 Absorbable Polydioxanone Surgical Suture