CONFIANZA PRO 8-20 300cm Pre-shape

GUDID 14547327138878

ASAHI INTECC CO., LTD.

Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use

• Primary Device ID: 14547327138878
• NIH Device Record Key: d8b5e63c-e4e1-4fdc-b845-6b78207446cf
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: CONFIANZA PRO 8-20 300cm Pre-shape
• Version Model Number: AGH143392P
• Company DUNS: 690711189
• Company Name: ASAHI INTECC CO., LTD.
• 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: 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 Dimensions

• Length: 300 Centimeter
• Outer Diameter: 0.014 Inch
• Length: 300 Centimeter
• Outer Diameter: 0.014 Inch
• Length: 300 Centimeter
• Outer Diameter: 0.014 Inch
• Length: 300 Centimeter
• Outer Diameter: 0.014 Inch
• Length: 300 Centimeter
• Outer Diameter: 0.014 Inch
• Length: 300 Centimeter
• Outer Diameter: 0.014 Inch
• Length: 300 Centimeter
• Outer Diameter: 0.014 Inch
• Length: 300 Centimeter
• Outer Diameter: 0.014 Inch
• Length: 300 Centimeter
• Outer Diameter: 0.014 Inch
• Length: 300 Centimeter
• Outer Diameter: 0.014 Inch
• Length: 300 Centimeter
• Outer Diameter: 0.014 Inch
• Length: 300 Centimeter
• Outer Diameter: 0.014 Inch
• Length: 300 Centimeter
• Outer Diameter: 0.014 Inch
• Length: 300 Centimeter
• Outer Diameter: 0.014 Inch
• Length: 300 Centimeter
• Outer Diameter: 0.014 Inch
• Length: 300 Centimeter
• Outer Diameter: 0.014 Inch

Device Identifiers

Device Issuing Agency	Device ID
GS1	04547327138871 [Primary]
GS1	14547327138878 [Package]; Contains: 04547327138871; Package: [5 Units]; In Commercial Distribution

FDA Product Code

• DQX: Wire, guide, catheter

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2022-01-24
• Device Publish Date: 2022-01-16

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