XIAN WANLI

GUDID 06973888820005

Hubei Wanli Protective Products Co.,Ltd

Surgical/medical face mask, non-antimicrobial, single-use

• Primary Device ID: 06973888820005
• NIH Device Record Key: 601dce47-d965-481c-af05-9a1f2ee9cada
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: XIAN WANLI
• Version Model Number: WLM2002
• Company DUNS: 527797615
• Company Name: Hubei Wanli Protective Products 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: 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: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	06973888820005 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K210150

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: 2023-08-04
• Device Publish Date: 2023-07-27