Belifu

GUDID 04895045403819

Grandway Technology (Shenzhen) Limited

Automatic-inflation electronic sphygmomanometer, portable, arm/wrist

• Primary Device ID: 04895045403819
• NIH Device Record Key: e0527bdc-40b3-445c-adba-137c3039521e
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Belifu
• Version Model Number: MD3151
• Company DUNS: 420764247
• Company Name: Grandway Technology (Shenzhen) Limited
• 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: 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: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	04895045403819 [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: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2020-08-27
• Device Publish Date: 2020-08-19

Devices Manufactured by Grandway Technology (Shenzhen) Limited

• 04895045404021 - G.LAB: 2021-05-13
• 08534550072122 - G.LAB: 2021-02-02
• 04895045403819 - Belifu: 2020-08-27
• 04895045403819 - Belifu: 2020-08-27
• 04895045403598 - G.LAB: 2019-11-08
• 04895045403604 - G.LAB: 2019-11-08
• 04895045403611 - G.LAB: 2019-11-08
• 04895045403628 - G.LAB: 2019-11-08
• 04895045403635 - G.LAB: 2019-11-08