ARRIGO PROFESSIONAL SUPPLIES LLC

GUDID 00850072625201

Andon Health Co., Ltd.

Automatic-inflation electronic sphygmomanometer, portable, arm/wrist

• Primary Device ID: 00850072625201
• NIH Device Record Key: 85b4589d-995b-4ccf-882c-3b15e578ed8c
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ARRIGO PROFESSIONAL SUPPLIES LLC
• Version Model Number: KD-7920
• Company DUNS: 421785478
• Company Name: Andon Health Co., Ltd.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Unsafe
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: true
• Serial Number: false
• 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	00850072625201 [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: 2025-12-23
• Device Publish Date: 2025-12-15

On-Brand Devices [ARRIGO PROFESSIONAL SUPPLIES LLC]

• 00850072625232: PT2L
• 00850072625201: KD-7920
• 00850072625195: KD-5920TL