Up & Up

GUDID 20810125111888

TARGET CORPORATION

Intermittent electronic patient thermometer

• Primary Device ID: 20810125111888
• NIH Device Record Key: 14a5f561-85d0-433f-bcbc-ca157010e6bb
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Up & Up
• Version Model Number: DT003
• Company DUNS: 006961700
• Company Name: TARGET CORPORATION
• 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: true
• 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	00810125111884 [Primary]
GS1	20810125111888 [Package]; Contains: 00810125111884; Package: [72 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K163603

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: 2024-03-21
• Device Publish Date: 2024-03-13

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