CROSSLOOP

GUDID 14547327155363

ASAHI INTECC CO., LTD.

Peripheral vascular guidewire, manual

• Primary Device ID: 14547327155363
• NIH Device Record Key: 16f9b8e2-2e5b-4534-af8b-40814ffd163a
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: CROSSLOOP
• Version Model Number: LPM01820P
• 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

• Outer Diameter: 0.018 Inch
• Length: 200 Centimeter
• Outer Diameter: 0.018 Inch
• Length: 200 Centimeter
• Outer Diameter: 0.018 Inch
• Length: 200 Centimeter
• Outer Diameter: 0.018 Inch
• Length: 200 Centimeter
• Outer Diameter: 0.018 Inch
• Length: 200 Centimeter
• Outer Diameter: 0.018 Inch
• Length: 200 Centimeter
• Outer Diameter: 0.018 Inch
• Length: 200 Centimeter
• Outer Diameter: 0.018 Inch
• Length: 200 Centimeter
• Outer Diameter: 0.018 Inch
• Length: 200 Centimeter
• Outer Diameter: 0.018 Inch
• Length: 200 Centimeter
• Outer Diameter: 0.018 Inch
• Length: 200 Centimeter
• Outer Diameter: 0.018 Inch
• Length: 200 Centimeter
• Outer Diameter: 0.018 Inch
• Length: 200 Centimeter
• Outer Diameter: 0.018 Inch
• Length: 200 Centimeter
• Outer Diameter: 0.018 Inch
• Length: 200 Centimeter
• Outer Diameter: 0.018 Inch
• Length: 200 Centimeter
• Outer Diameter: 0.018 Inch
• Length: 200 Centimeter
• Outer Diameter: 0.018 Inch
• Length: 200 Centimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	04547327155366 [Primary]
GS1	14547327155363 [Package]; Contains: 04547327155366; 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: 2025-05-06
• Device Publish Date: 2025-04-28

On-Brand Devices [CROSSLOOP]

• 14547327155400: LPM01830P
• 14547327155394: LPM01830S
• 14547327155387: LPM01823P
• 14547327155370: LPM01823S
• 14547327155363: LPM01820P
• 14547327155356: LPM01820S