FIELDER FC

GUDID 14547327067949

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

• Primary Device ID: 14547327067949
• NIH Device Record Key: a81dd76e-7437-4243-9327-00baef5ea40d
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: FIELDER FC
• Version Model Number: AGP140301
• 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
• 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
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	04547327067942 [Primary]
GS1	14547327067949 [Package]; Contains: 04547327067942; 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: Update
• Device Record Status: Published
• Public Version Number: 5
• Public Version Date: 2019-11-22
• Device Publish Date: 2016-09-16

On-Brand Devices [FIELDER FC]

• 14547327076224: AGP140301J
• 14547327076217: AGP140001J
• 14547327067949: AGP140301
• 14547327067932: AGP140001