Cumbor

GUDID 06953825904524

Shenzhen Urion Technology Co., Ltd

Automatic-inflation electronic sphygmomanometer, portable, arm/wrist

• Primary Device ID: 06953825904524
• NIH Device Record Key: 5b8ce185-1a2f-4871-92a0-474c9e377ba0
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Cumbor
• Version Model Number: U80LH
• 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: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: true
• 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	06953825904524 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K160019

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: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2020-04-09
• Device Publish Date: 2018-08-23

Devices Manufactured by Shenzhen Urion Technology Co., Ltd

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• 16953825909304 - carda health: 2025-01-20
• 16953825909281 - VtsniMed: 2025-01-14
• 16953825909243 - EVOLUTI: 2025-01-13
• 16953825909236 - COCACIS: 2025-01-09
• 16953825909168 - N/A: 2024-12-26
• 26953825909097 - santecare: 2024-12-25
• 16953825909076 - Andesfit Health: 2024-12-13