lyob

GUDID 16953825910980

Shenzhen Urion Technology Co., Ltd

Automatic-inflation electronic sphygmomanometer, portable, arm/wrist

• Primary Device ID: 16953825910980
• NIH Device Record Key: 74c4314a-787c-431b-95b2-99625e3a615b
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: lyob
• Version Model Number: U86Y
• Company DUNS: 421294358
• Company Name: Shenzhen Urion 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: true
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: true
• Serial Number: false
• 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: true

Device Identifiers

Device Issuing Agency	Device ID
GS1	06953825910983 [Primary]
GS1	16953825910980 [Package]; Contains: 06953825910983; Package: Carton [40 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K243115

FDA Product Code

• DXN: System, Measurement, Blood-Pressure, Non-Invasive

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: 2026-03-30
• Device Publish Date: 2026-03-20

Devices Manufactured by Shenzhen Urion Technology Co., Ltd

• 16953825910980 - lyob: 2026-03-30
• 16953825910980 - lyob: 2026-03-30
• 16953825910966 - N/A: 2026-03-25
• 16953825910959 - N/A: 2026-03-17
• 06953825910914 - medisana: 2026-03-11
• 16953825910904 - SDUNW: 2026-02-24
• 16953825910843 - N/A: 2026-02-16
• 16953825910850 - medisana: 2026-02-16
• 16953825910829 - SAKER: 2026-02-02