Constellation®

GUDID 08714729780465

Multiple Electrode Recording and Pacing Catheter

BOSTON SCIENTIFIC CORPORATION

Cardiac mapping catheter, percutaneous, single-use

• Primary Device ID: 08714729780465
• NIH Device Record Key: e1fda03c-4e1f-4002-aad9-cc916827a590
• Commercial Distribution Discontinuation: 2022-01-27
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: Constellation®
• Version Model Number: M004US8060U0
• Company DUNS: 021717889
• Company Name: BOSTON SCIENTIFIC 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

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Device Identifiers

Device Issuing Agency	Device ID
GS1	08714729780465 [Primary]

FDA Product Code

• MTD: CATHETER,INTRACARDIAC MAPPING,HIGH-DENSITY ARRAY

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: 2024-10-03
• Device Publish Date: 2016-09-24

On-Brand Devices [Constellation®]

• 08714729780472: Multiple Electrode Recording and Pacing Catheter
• 08714729780465: Multiple Electrode Recording and Pacing Catheter
• 08714729780458: Multiple Electrode Recording and Pacing Catheter
• 08714729780441: Multiple Electrode Recording and Pacing Catheter
• 08714729780434: Multiple Electrode Recording and Pacing Catheter