CombiStar Plus Filter flex

GUDID 04048675714446

Drägerwerk AG & Co. KGaA

Breathing circuit catheter mount, single-use

• Primary Device ID: 04048675714446
• NIH Device Record Key: d28f2478-8362-4da1-a837-980ea8718564
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: CombiStar Plus Filter flex
• Version Model Number: MP12063
• 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: true
• 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	04048675714446 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K221836

FDA Product Code

• CAH: Filter, Bacterial, Breathing-Circuit

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

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