Kinetix™ Plus

GUDID 08714729784029

PTCA Guidewire

BOSTON SCIENTIFIC CORPORATION

Cardiac/peripheral vascular guidewire, single-use

• Primary Device ID: 08714729784029
• NIH Device Record Key: d6fa622e-962d-4089-81d6-777a7ab44270
• Commercial Distribution Discontinuation: 2020-04-22
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: Kinetix™ Plus
• Version Model Number: H74939122040
• Company DUNS: 021717889
• Company Name: BOSTON SCIENTIFIC CORPORATION
• 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

• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	08714729784012 [Primary]
GS1	08714729784029 [Package]; Contains: 08714729784012; Package: [5 Units]; Discontinued: 2020-04-22; Not 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: 3
• Public Version Date: 2025-12-05
• Device Publish Date: 2016-09-24

On-Brand Devices [Kinetix™ Plus]

• 08714729784043: PTCA Guidewire
• 08714729784029: PTCA Guidewire
• 08714729784005: PTCA Guidewire
• 08714729783985: PTCA Guidewire