Breath syst 22mm (Aktive Humid)Sili

GUDID 07325710002032

Maquet Critical Care AB

Ventilator breathing circuit, single-use

• Primary Device ID: 07325710002032
• NIH Device Record Key: 74dd59f2-39b4-426e-bb6d-2b6e4fdc7fab
• Commercial Distribution Discontinuation: 2019-09-10
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: Breath syst 22mm (Aktive Humid)Sili
• Version Model Number: 6691965
• Company DUNS: 632707092
• Company Name: Maquet Critical Care AB
• 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: false
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	07325710002032 [Primary]

FDA Product Code

• CAI: Circuit, Breathing (W Connector, Adaptor, Y Piece)

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2019-11-27
• Device Publish Date: 2015-10-30

Devices Manufactured by Maquet Critical Care AB

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• 07325710011607 - PiCCO catheter: 2026-04-01
• 07325710017043 - PiCCO catheter: 2026-04-01
• 07325710017067 - PiCCO catheter: 2026-04-01
• 07325710017098 - PiCCO catheter: 2026-04-01
• 07325710017104 - PiCCO catheter: 2026-04-01
• 07325710012673 - Drawer for Low mobile carts: 2023-12-18
• 07325710001653 - Compressor Mini 115V 60Hz: 2023-09-29