MEO

GUDID 06973114620300

17.5×9.5cm

Fujian MEO Medical Technology Ltd.

Surgical/medical face mask, single-use

• Primary Device ID: 06973114620300
• NIH Device Record Key: a2839108-29d0-444f-bad0-6259576fd282
• Commercial Distribution Discontinuation: 2056-08-18
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: MEO
• Version Model Number: 17.5×9.5
• Company DUNS: 554530265
• Company Name: Fujian MEO Medical Technology 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: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: true
• 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	06973114620300 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K210870

FDA Product Code

• FXX: Mask, Surgical

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: 2022-01-21
• Device Publish Date: 2022-01-13