Maestro 4000™ Controller

GUDID 08714729861935

RF Cardiac Ablation Controller

BOSTON SCIENTIFIC CORPORATION

Percutaneous radio-frequency ablation system generator

• Primary Device ID: 08714729861935
• NIH Device Record Key: 4aa81a09-04b9-4b6c-a1a0-c21c955fa154
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Maestro 4000™ Controller
• Version Model Number: M0044000H0
• 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: false
• Lot Batch: false
• Serial Number: true
• Manufacturing Date: true
• Expiration Date: false
• 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	08714729861935 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Approval: P020025

FDA Product Code

• LPB: Cardiac ablation percutaneous catheter

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2022-06-10
• Device Publish Date: 2018-03-19

On-Brand Devices [Maestro 4000™ Controller]

• 08714729861942: RF Cardiac Ablation Controller
• 08714729861935: RF Cardiac Ablation Controller
• 08714729861928: RF Cardiac Ablation Controller
• 08714729861911: RF Cardiac Ablation Controller