InspiraChamber®

GUDID 05023323029829

InspiraChamber® Anti-Static Valved Holding Chamber + Large InspiraMask™

CLEMENT CLARKE INTERNATIONAL LIMITED

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• Primary Device ID: 05023323029829
• NIH Device Record Key: 154c84b1-2791-4900-bf03-a9a7448f5885
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: InspiraChamber®
• Version Model Number: 100110L
• Company DUNS: 216155952
• Company Name: CLEMENT CLARKE INTERNATIONAL 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	00327437043012 [Previous]
GS1	05023323029829 [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: 2024-06-06
• Device Publish Date: 2024-05-29

On-Brand Devices [InspiraChamber® ]

• 05023323029782: InspiraChamber® Anti-Static Valved Holding Chamber
• 05023323029768: InspiraChamber® Anti-Static Valved Holding Chamber
• 05023323029829: InspiraChamber® Anti-Static Valved Holding Chamber + Large InspiraMask™
• 05023323029812: InspiraChamber® Anti-Static Valved Holding Chamber + Medium InspiraMask™
• 05023323029799: InspiraChamber® Anti-Static Valved Holding Chamber + Small InspiraMask™