70102.5155

GUDID 04037691022468

Venous Catheter, wire reinforced with Full Lumen tip, 90° bent

Maquet Cardiopulmonary AG

Cardiopulmonary bypass cannula, venous

• Primary Device ID: 04037691022468
• NIH Device Record Key: f58dd014-656f-4a03-b796-9755270c9f9e
• Commercial Distribution Discontinuation: 2020-01-31
• Commercial Distribution Status: Not in Commercial Distribution
• Version Model Number: Ven.Cath.,reinf.,F.Lumen tip,90°bent
• Catalog Number: 70102.5155
• 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
• 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
• 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

• Device Size Text, specify: 0
• Catheter Gauge: 32 French
• Device Size Text, specify: 0
• Length: 40 Centimeter
• Device Size Text, specify: 0
• Catheter Gauge: 32 French
• Device Size Text, specify: 0
• Length: 40 Centimeter
• Device Size Text, specify: 0
• Catheter Gauge: 32 French
• Device Size Text, specify: 0
• Length: 40 Centimeter
• Device Size Text, specify: 0
• Catheter Gauge: 32 French
• Device Size Text, specify: 0
• Length: 40 Centimeter
• Device Size Text, specify: 0
• Catheter Gauge: 32 French
• Device Size Text, specify: 0
• Length: 40 Centimeter
• Device Size Text, specify: 0
• Catheter Gauge: 32 French
• Device Size Text, specify: 0
• Length: 40 Centimeter
• Device Size Text, specify: 0
• Catheter Gauge: 32 French
• Device Size Text, specify: 0
• Length: 40 Centimeter
• Device Size Text, specify: 0
• Catheter Gauge: 32 French
• Device Size Text, specify: 0
• Length: 40 Centimeter
• Device Size Text, specify: 0
• Catheter Gauge: 32 French
• Device Size Text, specify: 0
• Length: 40 Centimeter
• Device Size Text, specify: 0
• Catheter Gauge: 32 French
• Device Size Text, specify: 0
• Length: 40 Centimeter
• Device Size Text, specify: 0
• Catheter Gauge: 32 French
• Device Size Text, specify: 0
• Length: 40 Centimeter
• Device Size Text, specify: 0
• Catheter Gauge: 32 French
• Device Size Text, specify: 0
• Length: 40 Centimeter
• Device Size Text, specify: 0
• Catheter Gauge: 32 French
• Device Size Text, specify: 0
• Length: 40 Centimeter
• Device Size Text, specify: 0
• Catheter Gauge: 32 French
• Device Size Text, specify: 0
• Length: 40 Centimeter
• Device Size Text, specify: 0
• Catheter Gauge: 32 French
• Device Size Text, specify: 0
• Length: 40 Centimeter
• Device Size Text, specify: 0
• Catheter Gauge: 32 French
• Device Size Text, specify: 0
• Length: 40 Centimeter
• Device Size Text, specify: 0
• Catheter Gauge: 32 French
• Device Size Text, specify: 0
• Length: 40 Centimeter
• Device Size Text, specify: 0
• Catheter Gauge: 32 French
• Device Size Text, specify: 0
• Length: 40 Centimeter
• Device Size Text, specify: 0
• Catheter Gauge: 32 French
• Device Size Text, specify: 0
• Length: 40 Centimeter
• Device Size Text, specify: 0
• Catheter Gauge: 32 French
• Device Size Text, specify: 0
• Length: 40 Centimeter
• Device Size Text, specify: 0
• Catheter Gauge: 32 French
• Device Size Text, specify: 0
• Length: 40 Centimeter
• Device Size Text, specify: 0
• Catheter Gauge: 32 French
• Device Size Text, specify: 0
• Length: 40 Centimeter
• Device Size Text, specify: 0
• Catheter Gauge: 32 French
• Device Size Text, specify: 0
• Length: 40 Centimeter
• Device Size Text, specify: 0
• Catheter Gauge: 32 French
• Device Size Text, specify: 0
• Length: 40 Centimeter
• Device Size Text, specify: 0
• Catheter Gauge: 32 French
• Device Size Text, specify: 0
• Length: 40 Centimeter
• Device Size Text, specify: 0
• Catheter Gauge: 32 French
• Device Size Text, specify: 0
• Length: 40 Centimeter
• Device Size Text, specify: 0
• Catheter Gauge: 32 French
• Device Size Text, specify: 0
• Length: 40 Centimeter
• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	04037691022468 [Package]; Contains: 04037691237831; Package: [10 Units]; Discontinued: 2020-01-31; Not in Commercial Distribution
GS1	04037691237831 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K872182

FDA Product Code

• DQY: CATHETER, PERCUTANEOUS

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 5
• Public Version Date: 2020-01-31
• Device Publish Date: 2015-10-24

Devices Manufactured by Maquet Cardiopulmonary AG

• 04037691002583 - NA: 2024-09-30
• 04037691349190 - BMU 40: 2024-09-30
• 04037691349206 - BMU 40: 2024-09-30
• 04037691349213 - BMU 40: 2024-09-30
• 04037691349220 - BMU 40: 2024-09-30
• 04037691349237 - BMU 40: 2024-09-30
• 04037691349244 - BMU 40: 2024-09-30
• 04037691456584 - NA: 2024-09-30 Wall holder for ambulance. Mandatory for ambulance transportation.