arboleaf

GUDID 06928081772422

Shenzhen Yolanda Technology Co.,Ltd.

Automatic-inflation electronic sphygmomanometer, portable, arm/wrist

• Primary Device ID: 06928081772422
• NIH Device Record Key: 14117001-a962-4229-b1f5-6069461d79ba
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: arboleaf
• Version Model Number: SP20B
• Company DUNS: 421347580
• Company Name: Shenzhen Yolanda 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	06928081772422 [Primary]
GS1	16928081772429 [Package]; Package: [24 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K230176

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: 2025-04-22
• Device Publish Date: 2025-04-14

On-Brand Devices [arboleaf]

• 16928081771293: CS20W
• 16928081771255: SP10A
• 16928081771361: CS20M
• 06928081772422: SP20B
• 16928081771378: CS20N
• 06928081772651: CM20F
• 06928081771449: CM20C