Guide Wire 3mm J Tip 0.025" x 175 cm PTFE Coated (Type L) Fixed core 0684-00-0254-14

GUDID 10607567106601

Guide Wire 3mm J Tip 0.025" x 175 cm PTFE Coated (Type L) Fixed core

DATASCOPE CORP.

Cardiac/peripheral vascular guidewire, single-use

• Primary Device ID: 10607567106601
• NIH Device Record Key: 3b836407-a9b0-4e6e-a667-c21420013bfc
• Commercial Distribution Discontinuation: 2024-03-31
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: Guide Wire 3mm J Tip 0.025" x 175 cm PTFE Coated (Type L) Fixed core
• Version Model Number: 0684-00-0254-14
• Catalog Number: 0684-00-0254-14
• 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: 888-627-8383
• Email: customer.support@maquet.com
• Phone: 888-627-8383
• Email: customer.support@maquet.com
• Phone: 888-627-8383
• Email: customer.support@maquet.com
• Phone: 888-627-8383
• Email: customer.support@maquet.com
• Phone: 888-627-8383
• Email: customer.support@maquet.com
• Phone: 888-627-8383
• Email: customer.support@maquet.com
• Phone: 888-627-8383
• Email: customer.support@maquet.com
• Phone: 888-627-8383
• Email: customer.support@maquet.com
• Phone: 888-627-8383
• Email: customer.support@maquet.com
• Phone: 888-627-8383
• Email: customer.support@maquet.com
• Phone: 888-627-8383
• Email: customer.support@maquet.com
• Phone: 888-627-8383
• Email: customer.support@maquet.com

Device Dimensions

• Outer Diameter: 0.025 Inch
• Length: 175 Centimeter
• Outer Diameter: 0.025 Inch
• Length: 175 Centimeter
• Outer Diameter: 0.025 Inch
• Length: 175 Centimeter
• Outer Diameter: 0.025 Inch
• Length: 175 Centimeter
• Outer Diameter: 0.025 Inch
• Length: 175 Centimeter
• Outer Diameter: 0.025 Inch
• Length: 175 Centimeter
• Outer Diameter: 0.025 Inch
• Length: 175 Centimeter
• Outer Diameter: 0.025 Inch
• Length: 175 Centimeter
• Outer Diameter: 0.025 Inch
• Length: 175 Centimeter
• Outer Diameter: 0.025 Inch
• Length: 175 Centimeter
• Outer Diameter: 0.025 Inch
• Length: 175 Centimeter
• Outer Diameter: 0.025 Inch
• Length: 175 Centimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	10607567106601 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K943896

FDA Product Code

• DQX: Wire, Guide, Catheter

Sterilization

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

[10607567106601]

Ethylene Oxide

[10607567106601]

Ethylene Oxide

[10607567106601]

Ethylene Oxide

[10607567106601]

Ethylene Oxide

[10607567106601]

Ethylene Oxide

[10607567106601]

Ethylene Oxide

[10607567106601]

Ethylene Oxide

[10607567106601]

Ethylene Oxide

[10607567106601]

Ethylene Oxide

[10607567106601]

Ethylene Oxide

[10607567106601]

Ethylene Oxide

[10607567106601]

Ethylene Oxide

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2024-11-22
• Device Publish Date: 2016-09-23

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