VeriSmart

GUDID 06970389630348

Famidoc Technology Co.,Ltd.

Automatic-inflation electronic sphygmomanometer, portable, arm/wrist

• Primary Device ID: 06970389630348
• NIH Device Record Key: 857d33aa-12eb-40e1-943f-223c7bbd8fe0
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: VeriSmart
• Version Model Number: VSH-B550
• Company DUNS: 421343701
• Company Name: Famidoc Technology 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	06970389630348 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K191673

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: 2025-07-01
• Device Publish Date: 2025-06-23

Devices Manufactured by Famidoc Technology Co.,Ltd.

• 06970389630348 - VeriSmart: 2025-07-01
• 06970389630348 - VeriSmart: 2025-07-01
• 06970389630898 - EQUATE: 2025-03-12 TENS & EMS Pain Therapy Device
• 06970389631130 - Famidoc: 2023-10-02
• 06970389632335 - Famidoc: 2023-10-02
• 06970389634001 - Famidoc: 2023-10-02
• 06970389634025 - Famidoc: 2023-10-02
• 06970389634032 - Famidoc: 2023-10-02
• 06970389634056 - Famidoc: 2023-10-02