GUDID 06972040110817

Shenzhen AOJ Medical Technology Co., Ltd

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• Primary Device ID: 06972040110817
• NIH Device Record Key: 700b1ada-449f-40ae-af42-c59a32f5f27c
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: LZL-HA101
• 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: 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	06972040110817 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K222125

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: 2023-04-03
• Device Publish Date: 2023-03-24

Devices Manufactured by Shenzhen AOJ Medical Technology Co., Ltd

• 00628719266038 - Path Pharm: 2024-01-26
• 06972040112392 - frida baby: 2024-01-22
• 06972040110817 - NA: 2023-04-03
• 06972040110817 - NA: 2023-04-03
• 06972040111456 - fridababy: 2022-11-08
• 06972040111432 - fridababy: 2022-10-26
• 06972040111166 - ANMEATE: 2022-03-28
• 06972040111067 - MediBio: 2022-03-24
• 06972040110794 - Electronic Blood Pressure Monitor: 2021-11-08 The Electronic Blood Pressure Monitor is intended to measure the systolic and diastolic blood pressure as well as the pulse rate