ASAHI Corsair Pro XS

GUDID 04547327123679

ASAHI INTECC CO., LTD.

Vascular microcatheter

• Primary Device ID: 04547327123679
• NIH Device Record Key: 501e60db-ac52-41fd-8bee-5351864ce295
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ASAHI Corsair Pro XS
• Version Model Number: CSR150-21S
• 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: 150 Centimeter
• Length: 150 Centimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	04547327123679 [Primary]

FDA Product Code

• DQY: Catheter, percutaneous

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: 2019-01-25

On-Brand Devices [ASAHI Corsair Pro XS]

• 04547327123679: CSR150-21S
• 04547327123662: CSR135-21S