Karma

GUDID 08059173396474

QUANTA SYSTEM SPA

Dermatological frequency-doubled solid-state laser system

• Primary Device ID: 08059173396474
• NIH Device Record Key: 4a6c28da-ebaa-4479-9773-d07fd85d0c75
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Karma
• Version Model Number: PCMS00355
• Company DUNS: 436045833
• Company Name: QUANTA SYSTEM SPA
• 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: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	08059173396474 [Primary]

FDA Product Code

• GEX: Powered Laser Surgical Instrument

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: 2023-12-21
• Device Publish Date: 2023-12-13

Devices Manufactured by QUANTA SYSTEM SPA

• 08059173392186 - Litho EVO: 2025-10-07
• 08059173396375 - Echo: 2024-07-01
• 08033945936938 - Laserlith I-dust: 2024-05-23 Manufactured for Edap TMS
• 08059173396474 - Karma: 2023-12-21
• 08059173396474 - Karma: 2023-12-21
• 08059173396399 - Rosso: 2023-06-23
• 08059173396405 - Rosso: 2023-06-23
• 08033945934767 - Quantabella: 2023-06-16
• 08033945937492 - Litho 60: 2023-06-16