RITE AID

GUDID 10011822009055

MICROLIFE USA, INC.

Automatic-inflation electronic sphygmomanometer, portable, arm/wrist Automatic-inflation electronic sphygmomanometer, portable, arm/wrist Automatic-inflation electronic sphygmomanometer, portable, arm/wrist Automatic-inflation electronic sphygmomanometer, portable, arm/wrist Automatic-inflation electronic sphygmomanometer, portable, arm/wrist Automatic-inflation electronic sphygmomanometer, portable, arm/wrist Automatic-inflation electronic sphygmomanometer, portable, arm/wrist Automatic-inflation electronic sphygmomanometer, portable, arm/wrist Automatic-inflation electronic sphygmomanometer, portable, arm/wrist Automatic-inflation electronic sphygmomanometer, portable, arm/wrist Automatic-inflation electronic sphygmomanometer, portable, arm/wrist Automatic-inflation electronic sphygmomanometer, portable, arm/wrist Automatic-inflation electronic sphygmomanometer, portable, arm/wrist Automatic-inflation electronic sphygmomanometer, portable, arm/wrist Automatic-inflation electronic sphygmomanometer, portable, arm/wrist Automatic-inflation electronic sphygmomanometer, portable, arm/wrist Automatic-inflation electronic sphygmomanometer, portable, arm/wrist

• Primary Device ID: 10011822009055
• NIH Device Record Key: 2f5c7075-334b-436d-b45e-8c5ff0a31331
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: RITE AID
• Version Model Number: BP3KA1-1ERA
• Company DUNS: 176387785
• Company Name: MICROLIFE USA, 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: 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	00011822009058 [Primary]
GS1	10011822009055 [Package]; Contains: 00011822009058; Package: Box packing [6 Units]; In Commercial Distribution

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: 2023-08-21
• Device Publish Date: 2023-08-11

On-Brand Devices [RITE AID]

• 10011822622353: BP3NU1-3ERITE
• 10011822589946: BPAG1-20RITE
• 10011822514092: BP3AR1-4XRITE
• 10011822489338: BP3AR1-4DRITE (0348933)
• 10011822489321: BP3AQ1-1RITE
• 00011822002981: BP3KM1-3NRA
• 10011822009055: BP3KA1-1ERA
• 10011822009086: BP3KT1-4BRA
• 10011822009062: BP3KT1-3FRA
• 10011822009079: BP3GK1-3FRA