AirRay

GUDID 08800040900160

Poskom Co., Ltd.

Diagnostic x-ray system generator, portable

• Primary Device ID: 08800040900160
• NIH Device Record Key: c66f4e65-1ef4-4f82-bdc9-56167796222a
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: AirRay
• Version Model Number: AirRay-20HLW
• Company DUNS: 688458491
• Company Name: Poskom 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: 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	08800040900160 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K222896

FDA Product Code

• IZL: System, X-Ray, Mobile

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: 2023-06-23
• Device Publish Date: 2023-06-15

On-Brand Devices [AirRay]

• 08800040900160: AirRay-20HLW
• 08800040900153: AirRay-20HW
• 08800040900146: AirRay-20HL
• 08800040900139: AirRay-20H