Ensite™ H700295

GUDID 05415067002952

Catheter Catalog Installation

ST. JUDE MEDICAL, INC.

Cardiac mapping system application software

• Primary Device ID: 05415067002952
• NIH Device Record Key: ee460195-4927-403b-962d-19332f147f79
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Ensite™
• Version Model Number: Velocity™
• Catalog Number: H700295
• Company DUNS: 149818952
• Company Name: ST. JUDE MEDICAL, INC.
• 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: true
• Serial Number: false
• Manufacturing Date: true
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: true

Customer Support Contacts

• Phone: +1(855)478-5833
• Email: customerservice@sjm.com

Operating and Storage Conditions

• Special Storage Condition, Specify: Between 0 and 0 *Keep dry. Do not use if package is damaged.

Device Identifiers

Device Issuing Agency	Device ID
GS1	05415067002952 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K141050

FDA Product Code

• DQK: COMPUTER, DIAGNOSTIC, PROGRAMMABLE

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2016-04-21

On-Brand Devices [Ensite™]

• 05415067026200: Software Upgrade Kit, 30 day license, v.2.0
• 05415067026194: Software Upgrade Kit, v.2.0
• 05415067026163: Module, 30 day trial, v.1.0
• 05415067026132: Module, v.1.0
• 05415067024909: Noise Reduction Transformer, 100V
• 05415067024848: Noise Reduction Transformer, 120V
• 05415067024831: Noise Reduction Transformer, 240V
• 05415067014856: Software Upgrade Kit
• 05415067014573: Amplifier and Display Workstation
• 05415067012173: GenConnect Kit Stockert
• 05415067005861: Kit
• 05415067003867: Software Upgrade Kit
• 05415067003027: Software Installation
• 05415067002952: Catheter Catalog Installation
• 05415067002938: Catheter Catalog Installation
• 05415067002921: Catheter Catalog Installation
• 05415067001863: Software Installation
• 05415067001856: Software Upgrade Kit v.3.1
• 05415067001054: Display Workstation (DWS)
• 05415067000910: Display Workstation
• 05414734219211: Software Upgrade Kit v.3.0.1.1
• 15414734215661: Multi-electrode Diagnostic Catheter
• 05414734214841: Fusion™ Module
• 05414734214636: Fusion™ Module
• 05414734214469: Ablation Cable Kit, IBI,T9
• 05414734213738: 75-04630-002
• 05414734213684: Velocity™
• 05414734213660: Velocity™
• 05414734211246: Amplifier Kit
• 05414734211239: Display Workstation Kit
• 05414734210942: US Power Kit
• 05414734210713: Amplifier
• 05414734210614: Amplifier Kit
• 05414734210522: GenConnect Kit IBI
• 05414734210492: RecordConnect Kit Universal
• 05414734210188: Module
• 05415067000026: Kit, GenConnect, Stockert, NST
• 05414734210690: RecordConnect
• 05414734210546: GenConnect
• 05415067033185: Software License
• 05415067003041: DWS Kit
• 05414734210553: GenConnect
• 05414734210218: RecordConnect
• 05414734210201: EP-WorkMate RecordConnect
• 05414734210195: RecordConnect
• 05414734210706: Module
• 05414734209953: Module
• 05415067033789: Recording System Connector
• 05415067032300: Locating Electrodes
• 05415067031402: System Reference Electrode