VentiChamber

GUDID 05023323029997

VentiChamber + Medium VC Mask

CLEMENT CLARKE INTERNATIONAL LIMITED

Medicine chamber spacer, reusable

• Primary Device ID: 05023323029997
• NIH Device Record Key: 793422f8-3c8b-4596-be6d-8eb69bdd7429
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: VentiChamber
• Version Model Number: 036-01-020U
• 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	05023323029997 [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: 2024-10-15
• Device Publish Date: 2024-10-07

On-Brand Devices [VentiChamber]

• 05023323030054: VentiChamber (Box 50)
• 05023323030023: VentiChamber + Large VC Mask
• 05023323029997: VentiChamber + Medium VC Mask
• 05023323029973: VentiChamber + Small VC Mask
• 05023323029959: VentiChamber