Sejoy

GUDID 06970392211190

JOYTECH HEALTHCARE CO.,LTD

Intermittent electronic patient thermometer

• Primary Device ID: 06970392211190
• NIH Device Record Key: b2f2af8f-3d7e-4180-b1fa-8cf82fd61332
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Sejoy
• Version Model Number: DMT-1031
• 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: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	06970392211190 [Primary]

FDA Product Code

• FLL: Thermometer, Electronic, Clinical

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: 2020-06-29
• Device Publish Date: 2020-06-19

On-Brand Devices [Sejoy]

• 06970392215631: DET-306
• 06970392212319: DMT-102
• 06970392211190: DMT-1031
• 06970392210261: DMT412