Linear 7.5Fr 25cc IAB with Accessories (APA) (Turkey) 0684-00-0478-10

GUDID 10607567113210

Linear 7.5Fr 25cc IAB with Accessories (APA) (Turkey)

DATASCOPE CORP.

Intra-aortic balloon catheter

• Primary Device ID: 10607567113210
• NIH Device Record Key: fdf6153a-28f3-432d-9006-94209e080781
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Linear 7.5Fr 25cc IAB with Accessories (APA) (Turkey)
• Version Model Number: 0684-00-0478-10
• Catalog Number: 0684-00-0478-10
• Company DUNS: 001660786
• Company Name: DATASCOPE CORP.
• 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: true
• 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: 8886278383
• Email: customer.support@maquet.com
• Phone: 8886278383
• Email: customer.support@maquet.com
• Phone: 8886278383
• Email: customer.support@maquet.com
• Phone: 8886278383
• Email: customer.support@maquet.com
• Phone: 8886278383
• Email: customer.support@maquet.com
• Phone: 8886278383
• Email: customer.support@maquet.com
• Phone: 8886278383
• Email: customer.support@maquet.com
• Phone: 8886278383
• Email: customer.support@maquet.com
• Phone: 8886278383
• Email: customer.support@maquet.com
• Phone: 8886278383
• Email: customer.support@maquet.com
• Phone: 8886278383
• Email: customer.support@maquet.com
• Phone: 8886278383
• Email: customer.support@maquet.com
• Phone: 8886278383
• Email: customer.support@maquet.com
• Phone: 8886278383
• Email: customer.support@maquet.com
• Phone: 8886278383
• Email: customer.support@maquet.com
• Phone: 8886278383
• Email: customer.support@maquet.com
• Phone: 8886278383
• Email: customer.support@maquet.com

Device Dimensions

• Catheter Gauge: 7.5 French
• Catheter Gauge: 7.5 French
• Catheter Gauge: 7.5 French
• Catheter Gauge: 7.5 French
• Catheter Gauge: 7.5 French
• Catheter Gauge: 7.5 French
• Catheter Gauge: 7.5 French
• Catheter Gauge: 7.5 French
• Catheter Gauge: 7.5 French
• Catheter Gauge: 7.5 French
• Catheter Gauge: 7.5 French
• Catheter Gauge: 7.5 French
• Catheter Gauge: 7.5 French
• Catheter Gauge: 7.5 French
• Catheter Gauge: 7.5 French
• Catheter Gauge: 7.5 French
• Catheter Gauge: 7.5 French

Device Identifiers

Device Issuing Agency	Device ID
GS1	10607567113210 [Primary]

FDA Product Code

• DSP: System, Balloon, Intra-Aortic And Control

Sterilization

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

[10607567113210]

Ethylene Oxide

[10607567113210]

Ethylene Oxide

[10607567113210]

Ethylene Oxide

[10607567113210]

Ethylene Oxide

[10607567113210]

Ethylene Oxide

[10607567113210]

Ethylene Oxide

[10607567113210]

Ethylene Oxide

[10607567113210]

Ethylene Oxide

[10607567113210]

Ethylene Oxide

[10607567113210]

Ethylene Oxide

[10607567113210]

Ethylene Oxide

[10607567113210]

Ethylene Oxide

[10607567113210]

Ethylene Oxide

[10607567113210]

Ethylene Oxide

[10607567113210]

Ethylene Oxide

[10607567113210]

Ethylene Oxide

[10607567113210]

Ethylene Oxide

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2023-05-16
• Device Publish Date: 2023-05-08

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