RUNTHROUGH TW*AS430XA

GUDID 34987350703584

RUNTHROUGH NS Extra Floppy PTCA Guidewire

TERUMO CORPORATION

Cardiac/peripheral vascular guidewire, single-use

• Primary Device ID: 34987350703584
• NIH Device Record Key: 828165fd-c8e5-45bf-b8b6-32fff7540816
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: RUNTHROUGH
• Version Model Number: 25-1013
• Catalog Number: TW*AS430XA
• Company DUNS: 690543319
• Company Name: TERUMO CORPORATION
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Unsafe
• 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

Customer Support Contacts

• Phone: +1(800)283-7866
• Email: tmccustomer.admin@terumomedica

Device Dimensions

• Device Size Text, specify: 0
• Length: 300 Centimeter
• Outer Diameter: 0.36 Millimeter

Operating and Storage Conditions

• Special Storage Condition, Specify: Between 0 and 0 *Fragile. Keep dry. Keep away from sunlight. Stacking limit by 10.

Device Identifiers

Device Issuing Agency	Device ID
GS1	04987350703583 [Primary]
GS1	34987350703584 [Package]; Contains: 04987350703583; Package: Shelfbox [5 Units]; In Commercial Distribution
GS1	54987350703588 [Package]; Package: Carton [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: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2016-09-09

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