kiddieware

GUDID 16953825906181

Shenzhen Urion Technology Co., Ltd

Medical device pressure monitor

• Primary Device ID: 16953825906181
• NIH Device Record Key: 77d5aad4-65f1-45f0-8c67-f9353af21961
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: kiddieware
• Version Model Number: UFR201
• Company DUNS: 421294358
• Company Name: Shenzhen Urion 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: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• 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	06953825906184 [Primary]
GS1	16953825906181 [Package]; Contains: 06953825906184; Package: Carton [60 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K200802

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: 2022-08-10
• Device Publish Date: 2022-08-02

Devices Manufactured by Shenzhen Urion Technology Co., Ltd

• 16953825909700 - WEONY: 2025-05-12
• 16953825909717 - WEONY: 2025-05-12
• 16953825909724 - Aidisy: 2025-05-12
• 16953825906631 - Invaxe: 2025-05-09
• 16953825906662 - Healthpoint: 2025-05-09
• 16953825906723 - AccuCare: 2025-05-09
• 16953825906730 - ALPHAGOMED: 2025-05-09
• 16953825909694 - AlphaMed: 2025-05-09