KES

GUDID 06971513121022

Beijing KES Biology Technology Co.,Ltd.

Intense pulsed light skin surface treatment system Intense pulsed light skin surface treatment system Intense pulsed light skin surface treatment system Intense pulsed light skin surface treatment system Intense pulsed light skin surface treatment system Intense pulsed light skin surface treatment system Intense pulsed light skin surface treatment system Intense pulsed light skin surface treatment system Intense pulsed light skin surface treatment system Intense pulsed light skin surface treatment system Intense pulsed light skin surface treatment system Intense pulsed light skin surface treatment system Intense pulsed light skin surface treatment system Intense pulsed light skin surface treatment system Intense pulsed light skin surface treatment system Intense pulsed light skin surface treatment system Intense pulsed light skin surface treatment system Intense pulsed light skin surface treatment system Intense pulsed light skin surface treatment system Intense pulsed light skin surface treatment system Intense pulsed light skin surface treatment system Intense pulsed light skin surface treatment system Intense pulsed light skin surface treatment system Intense pulsed light skin surface treatment system Intense pulsed light skin surface treatment system Intense pulsed light skin surface treatment system

• Primary Device ID: 06971513121022
• NIH Device Record Key: d2931e31-9d7b-4791-9935-a517cb10cb38
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: KES
• Version Model Number: MED-230
• Company DUNS: 525608013
• Company Name: Beijing KES Biology Technology 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	06971513121022 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K122995

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: 2020-07-21
• Device Publish Date: 2020-07-13

On-Brand Devices [KES]

• 06971513121022: MED-230
• 06971513121039: MED-810A
• 06971513121015: MED-210
• 06971513121046: MED-808