sonmol

GUDID 06975038051017

Chongqing Moffy Innovation Technology Co., Ltd.

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• Primary Device ID: 06975038051017
• NIH Device Record Key: e50a4352-db3e-4145-ae69-c476d4f097d8
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: sonmol
• Version Model Number: SMPF-2S
• Company DUNS: 712614987
• Company Name: Chongqing Moffy Innovation Technology 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: false
• Lot Batch: true
• 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: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	06975038051017 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K203196

FDA Product Code

• BZH: Meter, Peak Flow, Spirometry

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: 2024-01-25
• Device Publish Date: 2024-01-17