AOJ

GUDID 06972040110183

Shenzhen AOJ Medical Technology Co., Ltd

Infrared patient thermometer, skin

• Primary Device ID: 06972040110183
• NIH Device Record Key: 91f67be3-db3e-4c88-ab26-d08d21ec5455
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: AOJ
• Version Model Number: AOJ-20E
• Company DUNS: 554409093
• Company Name: Shenzhen AOJ Medical 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: true
• Lot Batch: false
• 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	06972040110183 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K182133

FDA Product Code

• FLL: Thermometer, Electronic, Clinical

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2020-04-27
• Device Publish Date: 2019-10-16

On-Brand Devices [AOJ]

• 06972040110015: AOJ-20A
• 06972040110206: AOJ-20F
• 06972040110183: AOJ-20E
• 06972040110169: AOJ-20B
• 06972040110152: AOJ-20A
• 06972040110039: AOJ-20B