Double connector 11ID/15OD 20x

GUDID 04048675414520

Drägerwerk AG & Co. KGaA

Straight/elbow breathing circuit connector, single-use

• Primary Device ID: 04048675414520
• NIH Device Record Key: cdb9a8ba-4ce1-4b07-b327-8c99eccfabcc
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Double connector 11ID/15OD 20x
• Version Model Number: MP02655
• Company DUNS: 315578914
• Company Name: Drägerwerk AG & Co. KGaA
• 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: 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	04048675414520 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K222822

FDA Product Code

• BZE: Heater, Breathing System W/Wo Controller (Not Humidifier Or Nebulizer

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: 2023-07-31
• Device Publish Date: 2023-07-21

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