MICRO CIRRUS SMALL PARTICLE NEB

GUDID 05030267036707

MICRO CIRRUS SMALL PARTICLE NEB

INTERSURGICAL INCORPORATED

Nebulizing system delivery set, single-use

• Primary Device ID: 05030267036707
• NIH Device Record Key: d8e53a2c-0a4f-4c9a-9ab4-3304c29f836d
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: MICRO CIRRUS SMALL PARTICLE NEB
• Version Model Number: 1503130
• Company DUNS: 785952607
• Company Name: INTERSURGICAL INCORPORATED
• 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: true
• 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: false
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	05030267036707 [Package]; Contains: 05030267053322; Package: [100 Units]; In Commercial Distribution
GS1	05030267053322 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K911422

FDA Product Code

• CAF: Nebulizer (Direct Patient Interface)

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: 2021-10-12
• Device Publish Date: 2021-10-04

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