iWay

GUDID 06970005397013

Nasopharyngeal airway for oxygenation and capnography

Shenzhen Witleaf Medical Electronics Co., Ltd.

Nasopharyngeal airway, single-use

• Primary Device ID: 06970005397013
• NIH Device Record Key: c803bd96-194e-4322-bec6-6910c6fcc675
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: iWay
• Version Model Number: iway 13
• Company DUNS: 403635526
• Company Name: Shenzhen Witleaf Medical Electronics 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: 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: true
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	06970005397013 [Primary]

FDA Product Code

• BTQ: Airway, Nasopharyngeal

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: true

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2024-04-11
• Device Publish Date: 2024-04-03

On-Brand Devices [iWay ]

• 06970005397020: Nasopharyngeal airway for oxygenation and capnography
• 06970005397013: Nasopharyngeal airway for oxygenation and capnography