KOIOS

GUDID 16942284623043

JOYTECH HEALTHCARE CO.,LTD

Automatic-inflation electronic sphygmomanometer, portable, arm/wrist

• Primary Device ID: 16942284623043
• NIH Device Record Key: ad1acbac-ab0d-4816-a0b1-0ed17e3c4c94
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: KOIOS
• Version Model Number: DBP61C5
• Company DUNS: 544392778
• Company Name: JOYTECH HEALTHCARE CO.,LTD
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Safe
• 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: true
• 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	06942284623046 [Primary]
GS1	16942284623043 [Package]; Contains: 06942284623046; Package: [24 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: 2026-01-08
• Device Publish Date: 2025-12-31

On-Brand Devices [KOIOS]

• 16942284623036: DBP6175
• 16942284623043: DBP61C5