walgreens

GUDID 06973919590112

Shenzhen Teslong Technology Co.,Ltd

Otoscope, direct

• Primary Device ID: 06973919590112
• NIH Device Record Key: d6cf4b43-a627-44be-a067-dfa4c9b9c7cf
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: walgreens
• Version Model Number: 769379
• Company DUNS: 551471161
• Company Name: Shenzhen Teslong Technology Co.,Ltd
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• 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: true
• Manufacturing Date: false
• 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	06973919590112 [Primary]

FDA Product Code

• ERA: Otoscope

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: 2023-08-24
• Device Publish Date: 2023-08-16

Devices Manufactured by Shenzhen Teslong Technology Co.,Ltd

• 06973919590112 - walgreens: 2023-08-24
• 06973919590112 - walgreens: 2023-08-24
• 06973919590051 - Otoscope: 2023-07-07
• 06973919590068 - Otoscope: 2023-07-07
• 06973919590075 - Otoscope: 2023-07-07
• 06973919590082 - Otoscope: 2023-07-07
• 06973919590099 - Otoscope: 2023-07-07
• 06973919590105 - Otoscope: 2023-07-07