InspiraChamber®

GUDID 05023323029775

InspiraChamber® Anti-Static Valved Holding Chamber

FLEXICARE MEDICAL LIMITED

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• Primary Device ID: 05023323029775
• NIH Device Record Key: 6bc626d3-27bf-4531-9141-352c6e8f66a9
• Commercial Distribution Discontinuation: 2024-05-20
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: InspiraChamber®
• Version Model Number: 100150
• Company DUNS: 504406273
• Company Name: FLEXICARE MEDICAL LIMITED
• 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: false
• Manufacturing Date: true
• Expiration Date: false
• 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	00852367007068 [Previous]
GS1	05023323029775 [Primary]

FDA Product Code

• NVP: Holding Chambers, 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: 2024-05-27
• Device Publish Date: 2024-05-17

On-Brand Devices [InspiraChamber® ]

• 05023323029775: InspiraChamber® Anti-Static Valved Holding Chamber
• 05023323029751: InspiraChamber® Anti-Static Valved Holding Chamber