ASAHI SION

GUDID 14547327132968

ASAHI INTECC CO., LTD.

Cardiac/peripheral vascular guidewire, single-use

• Primary Device ID: 14547327132968
• NIH Device Record Key: 44b80c83-176f-4797-83fd-95d6a6e57777
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ASAHI SION
• Version Model Number: AHW14R101P
• 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: 0.014 Inch

Device Identifiers

Device Issuing Agency	Device ID
GS1	04547327132961 [Primary]
GS1	14547327132968 [Package]; Contains: 04547327132961; 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: 2019-12-16
• Device Publish Date: 2019-12-07

On-Brand Devices [ASAHI SION]

• 14547327086193: AHW14R301J
• 14547327086186: AHW14R001J
• 14547327082638: AHW14R301S
• 14547327082621: AHW14R001S
• 14547327133040: AHW14R101J
• 14547327132982: AHW14R101S
• 14547327132975: AHW14R301P
• 14547327132968: AHW14R101P