Fabius MRI

GUDID 04048675041498

Drägerwerk AG & Co. KGaA

Anaesthesia workstation, general-purpose

• Primary Device ID: 04048675041498
• NIH Device Record Key: 750edc80-0e03-4662-a9d1-db7b88f7effd
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Fabius MRI
• Version Model Number: 8607300
• Company DUNS: 315578914
• Company Name: Drägerwerk AG & Co. KGaA
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Safe
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: false
• Serial Number: true
• 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	04048675041498 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K072884

FDA Product Code

• BSZ: Gas-Machine, Anesthesia

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2015-10-24

Devices Manufactured by Drägerwerk AG & Co. KGaA

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• 04048675665762 - Filter SafeStar 90 Plus: 2026-01-23
• 04048675665786 - Filter SafeStar 60A Plus: 2026-01-23
• 04048675665823 - Filter/HME TwinStar HEPA Plus: 2026-01-23
• 04048675253426 - Mask NovaStarTS,NIV,w/SE,L: 2026-01-16
• 04048675253402 - Mask NovaStarTS,NIV,w/SE,S: 2026-01-16
• 04048675253419 - Mask NovaStarTS,NIV,w/SE,M: 2026-01-16