WARMLIFE

GUDID 06953825901776

Shenzhen Urion Technology Co., Ltd

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• Primary Device ID: 06953825901776
• NIH Device Record Key: c77a7470-81b5-4a2d-afd0-a24835148cac
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: WARMLIFE
• Version Model Number: U80AH
• 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	06953825901776 [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: 6
• Public Version Date: 2020-04-09
• Device Publish Date: 2016-09-19

On-Brand Devices [WARMLIFE]

• 06953825902773: U80EH
• 06953825901776: U80AH