70100.2241

GUDID 04037691056692

Arterial Cannula, wire reinforced, straight tip with flange

Maquet Cardiopulmonary AG

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• Primary Device ID: 04037691056692
• NIH Device Record Key: f95a159b-5d14-4ef7-991f-fd41c0735efb
• Commercial Distribution Discontinuation: 2020-01-31
• Commercial Distribution Status: Not in Commercial Distribution
• Version Model Number: Art.Can.,reinf.,straight tip w.flange
• Catalog Number: 70100.2241
• Company DUNS: 316153865
• Company Name: Maquet Cardiopulmonary AG
• 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: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +49072229320
• Email: info.cp@maquet.com
• Phone: +49072229320
• Email: info.cp@maquet.com
• Phone: +49072229320
• Email: info.cp@maquet.com
• Phone: +49072229320
• Email: info.cp@maquet.com
• Phone: +49072229320
• Email: info.cp@maquet.com
• Phone: +49072229320
• Email: info.cp@maquet.com
• Phone: +49072229320
• Email: info.cp@maquet.com
• Phone: +49072229320
• Email: info.cp@maquet.com
• Phone: +49072229320
• Email: info.cp@maquet.com
• Phone: +49072229320
• Email: info.cp@maquet.com
• Phone: +49072229320
• Email: info.cp@maquet.com
• Phone: +49072229320
• Email: info.cp@maquet.com

Device Dimensions

• Length: 23 Centimeter
• Catheter Gauge: 22 French
• Device Size Text, specify: 0
• Length: 23 Centimeter
• Catheter Gauge: 22 French
• Device Size Text, specify: 0
• Length: 23 Centimeter
• Catheter Gauge: 22 French
• Device Size Text, specify: 0
• Length: 23 Centimeter
• Catheter Gauge: 22 French
• Device Size Text, specify: 0
• Length: 23 Centimeter
• Catheter Gauge: 22 French
• Device Size Text, specify: 0
• Length: 23 Centimeter
• Catheter Gauge: 22 French
• Device Size Text, specify: 0
• Length: 23 Centimeter
• Catheter Gauge: 22 French
• Device Size Text, specify: 0
• Length: 23 Centimeter
• Catheter Gauge: 22 French
• Device Size Text, specify: 0
• Length: 23 Centimeter
• Catheter Gauge: 22 French
• Device Size Text, specify: 0
• Length: 23 Centimeter
• Catheter Gauge: 22 French
• Device Size Text, specify: 0
• Length: 23 Centimeter
• Catheter Gauge: 22 French
• Device Size Text, specify: 0
• Length: 23 Centimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	04037691056692 [Package]; Contains: 04037691239613; Package: [10 Units]; Discontinued: 2020-01-31; Not in Commercial Distribution
GS1	04037691239613 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K012774

FDA Product Code

• DWF: CATHETER, CANNULA AND TUBING, VASCULAR, CARDIOPULMONARY BYPASS

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2020-01-31
• Device Publish Date: 2015-10-24

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• 04037691576640 - Quadrox-iD: 2022-12-13
• 04037691588285 - HLS Set: 2022-12-13
• 04037691741130 - NA: 2022-12-08
• 04037691741543 - NA: 2022-12-08
• 04037691773513 - NA: 2022-12-08
• 04037691009025 - NA: 2022-12-06