TempBuddy

GUDID 06971209168010

Shenzhen Yuezhongxing Technology Co., Ltd.

Infrared patient thermometer, skin

• Primary Device ID: 06971209168010
• NIH Device Record Key: 8f395815-962b-4bfb-b673-24fade099bac
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: TempBuddy
• Version Model Number: ZTP-800
• Company DUNS: 418012517
• Company Name: Shenzhen Yuezhongxing Technology 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: true
• 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	06971209168010 [Primary]

FDA Product Code

• SDV: Clinical Electronic Thermometer

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: 2025-11-28
• Device Publish Date: 2025-11-20

Devices Manufactured by Shenzhen Yuezhongxing Technology Co., Ltd.

• 06971209168010 - TempBuddy: 2025-11-28
• 06971209168010 - TempBuddy: 2025-11-28
• 06971209162056 - MMIZOO: 2025-09-11
• 06971209161059 - Safety Wercs: 2023-12-01
• 06971209162025 - Safety Wercs: 2023-12-01
• 06971209160106 - Aleshon: 2023-07-27
• 06971209160113 - Aleshon: 2023-07-27
• 06971209160120 - Aleshon: 2023-07-27
• 06971209160137 - Aleshon: 2023-07-27