The Magnet™

GUDID 08714729008828

Exchange Device

BOSTON SCIENTIFIC CORPORATION

Catheter-exchange guidewire holder

• Primary Device ID: 08714729008828
• NIH Device Record Key: af1379e0-1ba3-4131-986c-78934365ea25
• Commercial Distribution Discontinuation: 2024-12-08
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: The Magnet™
• Version Model Number: H74908966050
• 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 Identifiers

Device Issuing Agency	Device ID
GS1	08714729008828 [Package]; Contains: 08714729724940; Package: [5 Units]; Discontinued: 2024-12-08; Not in Commercial Distribution
GS1	08714729724940 [Primary]

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: 2025-12-12
• Device Publish Date: 2016-09-24

On-Brand Devices [The Magnet™]

• 08714729008828: Exchange Device
• 08714729146841: Exchange Device