CREPINE DE LYSE CANNULA AL702

GUDID 03760037731588

AESTHETIC GROUP

Tissue injection cannula

• Primary Device ID: 03760037731588
• NIH Device Record Key: e1156c51-377b-486e-8d33-7dd29769d234
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: CREPINE DE LYSE CANNULA
• Version Model Number: 3mm x 15 cm - 10-hole
• Catalog Number: AL702
• Company DUNS: 260069352
• Company Name: AESTHETIC GROUP
• 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: 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: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	03760037731571 [Primary]
GS1	03760037731588 [Package]; Contains: 03760037731571; Package: Box [10 Units]; In Commercial Distribution

FDA Product Code

• GEA: Cannula, Surgical, General & Plastic Surgery
• MUU: System, Suction, Lipoplasty

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2019-12-12
• Device Publish Date: 2018-08-12

On-Brand Devices [CREPINE DE LYSE CANNULA]

• 03760037731588: 3mm x 15 cm - 10-hole
• 03760037731564: 3mm x 21 cm - 10-hole