Mericonn

GUDID 06975725491003

Shenzhen Mericonn Technology Co., Ltd

Foetal Doppler system

• Primary Device ID: 06975725491003
• NIH Device Record Key: f4e3457a-b16b-4d44-bae0-4fcca0638ebd
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Mericonn
• Version Model Number: FD200
• Company DUNS: 709546446
• Company Name: Shenzhen Mericonn 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: false
• Serial Number: false
• Manufacturing Date: true
• 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	06975725491003 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K212084

FDA Product Code

• KNG: Monitor, Ultrasonic, Fetal

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: 2024-07-17
• Device Publish Date: 2024-07-09

On-Brand Devices [Mericonn]

• 06975725492000: FD100
• 06975725494004: FD400
• 06975725493007: FD300
• 06975725491003: FD200