MTEHFYAF

GUDID 06975029700054

Beijing Xingjian Yongzhen Technology Co. , Ltd.

Rebreathing oxygen face mask

• Primary Device ID: 06975029700054
• NIH Device Record Key: 354b14e8-4a6a-461e-9574-f80af35756a8
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: MTEHFYAF
• Version Model Number: MY-FYY-03
• Company DUNS: 414510435
• Company Name: Beijing Xingjian Yongzhen 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: 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: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	06975029700054 [Primary]

FDA Product Code

• BYW: Device, Rebreathing

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: 2024-06-20
• Device Publish Date: 2024-06-12

On-Brand Devices [MTEHFYAF]

• 06975029700078: MY-QYJ-01
• 06975029700061: MY-FZS-01
• 06975029700054: MY-FYY-03