ASAHI Gaia Next 2

GUDID 14547327136300

ASAHI INTECC CO., LTD.

Cardiac/peripheral vascular guidewire, single-use

• Primary Device ID: 14547327136300
• NIH Device Record Key: a596dc32-b45a-4a84-ab1e-62bdaaec402f
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ASAHI Gaia Next 2
• Version Model Number: AH14R020P
• 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: 190 Centimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	04547327136303 [Primary]
GS1	14547327136300 [Package]; Contains: 04547327136303; 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: 2020-01-20
• Device Publish Date: 2020-01-10

On-Brand Devices [ASAHI Gaia Next 2]

• 14547327136300: AH14R020P
• 14547327142271: AH14R320P