Lightstuff

GUDID 26970392214898

JOYTECH HEALTHCARE CO.,LTD

Automatic-inflation electronic sphygmomanometer, portable, arm/wrist

• Primary Device ID: 26970392214898
• NIH Device Record Key: 845b0783-1f96-476a-8021-861862bd3160
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Lightstuff
• Version Model Number: DBP-2242
• Company DUNS: 544392778
• Company Name: JOYTECH HEALTHCARE 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: 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: true

Device Identifiers

Device Issuing Agency	Device ID
GS1	06970392214894 [Primary]
GS1	16970392214891 [Package]; Contains: 06970392214894; Package: [8 Units]; In Commercial Distribution
GS1	26970392214898 [Package]; Contains: 16970392214891; Package: [48 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: 2019-12-24
• Device Publish Date: 2019-12-16

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