Dynamic XT™ M0046DYNXT0020

GUDID 08714729879879

Unidirectional Steerable Diagnostic Catheter

BOSTON SCIENTIFIC CORPORATION

Cardiac mapping catheter, percutaneous, single-use

• Primary Device ID: 08714729879879
• NIH Device Record Key: 7ca2f3a3-bca2-4089-8350-173b7dd89e8b
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Dynamic XT™
• Version Model Number: M0046DYNXT0020
• Catalog Number: M0046DYNXT0020
• 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

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Device Identifiers

Device Issuing Agency	Device ID
GS1	08714729879879 [Primary]

FDA Product Code

• DRF: CATHETER, ELECTRODE RECORDING, OR PROBE, ELECTRODE RECORDING

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: 2025-12-03
• Device Publish Date: 2016-09-24

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