Anesthesia Circuit Kit Flex HEPA

GUDID 04048675695639

Drägerwerk AG & Co. KGaA

Anaesthesia breathing circuit, single-use

• Primary Device ID: 04048675695639
• NIH Device Record Key: 43afaf10-0e91-4c8c-9a75-a33b153d1d3e
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Anesthesia Circuit Kit Flex HEPA
• Version Model Number: MP17103
• Company DUNS: 315578914
• Company Name: Drägerwerk AG & Co. KGaA
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• 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	04048675695639 [Primary]

FDA Product Code

• OFP: Anesthesia Breathing Circuit Kit (Adult & Pediatric)

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: 2025-05-27
• Device Publish Date: 2025-05-19

Devices Manufactured by Drägerwerk AG & Co. KGaA

• 04048675428909 - ThermoTrace_Peripheral_5pcs: 2025-09-09
• 04048675428916 - ThermoTrace Core (5pcs): 2025-09-09
• 04048675695622 - Anesthesia Circuit Kit Coax HEPA: 2025-05-27
• 04048675695639 - Anesthesia Circuit Kit Flex HEPA: 2025-05-27
• 04048675695639 - Anesthesia Circuit Kit Flex HEPA: 2025-05-27
• 04048675686729 - VentStar Resus heated (N): 2025-05-22
• 04048675686743 - VentStar AutoBreath heated (N): 2025-05-22
• 04048675125525 - CLIC adapter: 2025-05-02
• 04048675379317 - ECG trunk cable,3-lead,Neo: 2025-04-18