CELLINEW

GUDID 08809502330347

VIOL Co.,Ltd.

Electrosurgical system

• Primary Device ID: 08809502330347
• NIH Device Record Key: 4853081c-1522-4b9b-b6cf-0bb0e2529ef9
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: CELLINEW
• Version Model Number: CELLINEW
• Company DUNS: 695654949
• Company Name: VIOL Co.,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: true
• Expiration Date: false
• 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	08809502330347 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K240897

FDA Product Code

• GEI: Electrosurgical, Cutting & Coagulation & Accessories

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: 2024-12-17
• Device Publish Date: 2024-12-09

Devices Manufactured by VIOL Co.,Ltd.

• 08809502330286 - CELLINEW Foot switch: 2024-12-17
• 08809502330347 - CELLINEW: 2024-12-17
• 08809502330347 - CELLINEW: 2024-12-17
• 08809502330361 - CELLINEW Handpiece: 2024-12-17
• 08809502330378 - CELLINEW TIP: 2024-12-17
• 08809502330385 - CELLINEW TIP: 2024-12-17
• 08809502330149 - XE25: 2022-07-07
• 08809502330156 - XA25: 2022-07-07
• 08809502330163 - XW18: 2022-07-07