Veridian

GUDID 10845717007655

JOYTECH HEALTHCARE CO.,LTD

Intermittent electronic patient thermometer

• Primary Device ID: 10845717007655
• NIH Device Record Key: 2e76461a-d994-4d74-b364-64e5e7dd2e22
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Veridian
• Version Model Number: 08-301VC
• 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	00845717007658 [Primary]
GS1	10845717007655 [Package]; Contains: 00845717007658; Package: [16 Units]; In Commercial Distribution

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: 2019-03-04
• Device Publish Date: 2019-01-30

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