Ultra Flex 1037060

GUDID 06970888440547

Laryngeal Mask Aiway Silicone Wire Reinforced Size 6.0

Jiangxi Yiles Medical Co., Ltd

Reinforced laryngeal mask airway, single-use

• Primary Device ID: 06970888440547
• NIH Device Record Key: 1f0206c4-a59b-46af-ab42-84d7cf9e5f35
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Ultra Flex
• Version Model Number: Size 6.0
• Catalog Number: 1037060
• Company DUNS: 561008872
• Company Name: Jiangxi Yiles Medical 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: true
• 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	06970888440547 [Primary]
GS1	16970888440544 [Package]; Package: [10 Units]; In Commercial Distribution

FDA Product Code

• CAE: Airway, Oropharyngeal, Anesthesiology

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: 2024-03-11
• Device Publish Date: 2024-03-02

On-Brand Devices [Ultra Flex]

• 06970888440547: Laryngeal Mask Aiway Silicone Wire Reinforced Size 6.0
• 16970888440537: Laryngeal Mask Aiway Silicone Wire Reinforced Size 5.0
• 16970888440520: Laryngeal Mask Aiway Silicone Wire Reinforced Size 4.0
• 16970888440513: Laryngeal Mask Aiway Silicone Wire Reinforced Size 3.0
• 16970888440506: Laryngeal Mask Aiway Silicone Wire Reinforced Size 2.5
• 16970888440490: Laryngeal Mask Aiway Silicone Wire Reinforced Size 2.0