Atlan A350

GUDID 04048675556176

Drägerwerk AG & Co. KGaA

Anaesthesia workstation, general-purpose

• Primary Device ID: 04048675556176
• NIH Device Record Key: b8b51a2c-cdee-4850-b2a4-d883f6e8d2c1
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Atlan A350
• Version Model Number: 8621500
• 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: 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	04048675556176 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K230931

FDA Product Code

• BSZ: Gas-Machine, Anesthesia

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: 2023-09-29
• Device Publish Date: 2023-09-21

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