Globalipl

GUDID 06973494935001

BEIJING GLOBALIPL DEVELOPMENT CO., LTD.

Intense pulsed light skin surface treatment system

• Primary Device ID: 06973494935001
• NIH Device Record Key: 46d13879-ebd4-42f0-a6bf-4c4f83f4ba60
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Globalipl
• Version Model Number: US500
• Company DUNS: 544936742
• Company Name: BEIJING GLOBALIPL DEVELOPMENT 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: 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	06973494935001 [Primary]

FDA Product Code

• ONF: Powered Light Based Non-Laser Surgical Instrument With Thermal Effect

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: 2022-08-24
• Device Publish Date: 2022-08-16

On-Brand Devices [Globalipl]

• 06973494934196: US419
• 06973494938019: US800N
• 06973494938002: US800
• 06973494935001: US500
• 06973494934509: US450