Kingon

GUDID 06971882890222

Qingdao Kingon Medical Science and Technology Co., Ltd

Mobile/portable oxygen concentrator

• Primary Device ID: 06971882890222
• NIH Device Record Key: 049bb191-8a49-49f0-bc6d-2ff90916424b
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Kingon
• Version Model Number: P2-S3
• Company DUNS: 554421353
• Company Name: Qingdao Kingon Medical Science and Technology Co., Ltd
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Unsafe
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: true
• 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	06971882890222 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K230702

FDA Product Code

• CAW: Generator, Oxygen, Portable

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: 2023-10-31
• Device Publish Date: 2023-10-23

On-Brand Devices [Kingon]

• 06971882890017: P2
• 06971882890093: P2-E6
• 06971882890109: P2-E
• 06971882890192: P2-E7
• 06971882890239: P2-S4
• 06971882890222: P2-S3
• 06971882890215: P2-K4
• 06971882890208: P2-K3
• 06971882890246: P2-E4