fridababy

GUDID 06972040111432

Shenzhen AOJ Medical Technology Co., Ltd

Intermittent electronic patient thermometer

• Primary Device ID: 06972040111432
• NIH Device Record Key: 83b26c5e-cfb5-4837-907e-dcb0da39f69d
• Commercial Distribution Discontinuation: 2023-04-18
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: fridababy
• Version Model Number: AOJ-25B
• Company DUNS: 554409093
• Company Name: Shenzhen AOJ Medical Technology Co., Ltd
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Safe
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: true
• Serial Number: true
• Manufacturing Date: true
• Expiration Date: true
• Donation Id Number: true
• 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	06972040111432 [Primary]

FDA Product Code

• DXN: System, Measurement, Blood-Pressure, Non-Invasive

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: 2022-10-26
• Device Publish Date: 2022-10-18

On-Brand Devices [fridababy]

• 00810028770614: FB068
• 06972040111432: AOJ-25B
• 06972040111456: AOJ-25B