BEBIRD

GUDID 06972403823781

Heifeng Zhizao(Shenzhen)Technology Co.,Ltd

Otoscope, direct

• Primary Device ID: 06972403823781
• NIH Device Record Key: 4bdd1e23-5dc1-41f2-918c-c4a803c93683
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: BEBIRD
• Version Model Number: M9 Pro
• Company DUNS: 554457316
• Company Name: Heifeng Zhizao(Shenzhen)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: true
• Serial Number: true
• Manufacturing Date: true
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: true
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	06972403823781 [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: 2021-10-01
• Device Publish Date: 2021-09-23

On-Brand Devices [BEBIRD]

• 06972403823798: W3-WM
• 06972403823781: M9 Pro
• 06972403823774: N3