UV Radiation Treatment System

GUDID 06921745209029

Xuzhou Yongkang Electronic Science Technology Co., Ltd

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• Primary Device ID: 06921745209029
• NIH Device Record Key: 98aa4d1a-b482-449b-a640-b22f9d369612
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: UV Radiation Treatment System
• Version Model Number: YK-6000B-T
• Company DUNS: 542753796
• Company Name: Xuzhou Yongkang Electronic Science Technology Co., Ltd
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• 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: true
• Serial Number: true
• Manufacturing Date: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: true
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	06921745209029 [Primary]

FDA Product Code

• FTC: Light, Ultraviolet, Dermatological

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: 2022-08-11
• Device Publish Date: 2022-08-03

Devices Manufactured by Xuzhou Yongkang Electronic Science Technology Co., Ltd

• 06921745209029 - UV Radiation Treatment System: 2022-08-11
• 06921745209029 - UV Radiation Treatment System: 2022-08-11
• 06921745200156 - yonker: 2019-11-08
• 06921745200026 - yonker: 2019-01-11 Fingertip Pulse Oximeter
• 06921745200033 - yonker: 2019-01-11 Fingertip Pulse Oximeter
• 06921745200163 - yonker: 2019-01-11 Wrist type Blood Pressure Monitor
• 06921745200255 - yonker: 2019-01-11 Fingertip Pulse Oximeter