Mask ClassicStar,NIV,SE,S

GUDID 04048675041115

Drägerwerk AG & Co. KGaA

Rebreathing oxygen face mask

• Primary Device ID: 04048675041115
• NIH Device Record Key: fa24239c-bec7-41d7-bac9-c10dd3552c14
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Mask ClassicStar,NIV,SE,S
• Version Model Number: MP01573
• Company DUNS: 315578914
• Company Name: Drägerwerk AG & Co. KGaA
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Unsafe
• 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: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +494518820
• Email: info@draeger.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	04048675041115 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K081743

FDA Product Code

• CBK: Ventilator, Continuous, Facility Use

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2018-07-06
• Device Publish Date: 2015-10-24

Devices Manufactured by Drägerwerk AG & Co. KGaA

• 04048675449119 - VentStar Oxylog 3000F,2000p 5x: 2024-12-13
• 04048675028987 - Angular porcelain bush: 2024-12-10
• 04048675180944 - Nozzle water vacuum gauge: 2024-12-10
• 04048675414605 - Silicone hose 6x2,5 2m: 2024-12-10
• 04048675692409 - Column/Head: 2024-12-10
• 04048675723035 - Vacusmart Tube (2m): 2024-12-10
• 04048675564553 - T-piece N for NO-A: 2024-10-16
• 04048675564577 - T-piece N for Nebulization: 2024-10-16