Sokkar

GUDID 00682891341006

BP Monitor UAM-410CA

ZEWA, INC.

Automatic-inflation electronic sphygmomanometer, portable, arm/wrist

• Primary Device ID: 00682891341006
• NIH Device Record Key: 2c03ea77-46dd-492b-a73a-21b782047006
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Sokkar
• Version Model Number: UAM-410CA
• Company DUNS: 013481078
• Company Name: ZEWA, INC.
• 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: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• 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	00682891341006 [Primary]

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: 2
• Public Version Date: 2019-11-08
• Device Publish Date: 2019-01-01

Devices Manufactured by ZEWA, INC.

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• 00682891390608 - Hello Heart: 2022-11-07 BP Monitor UAM-906HH
• 00682891395009 - Zewa: 2022-08-18 BP Monitor UAM-950
• 00682891213006 - Zewa: 2021-09-15 Scale
• 00682891390585 - Hello Heart: 2020-10-28 BP Monitor UAM-905MH
• 00682891390103 - Zewa: 2020-09-24 BP Monitor