LATITUDE Consult™

GUDID 00802526562907

LATITUDE Consult™ System

BOSTON SCIENTIFIC CORPORATION

Cardiac pulse generator software

• Primary Device ID: 00802526562907
• NIH Device Record Key: e3a7fb4a-4623-4764-b688-21683a834235
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: LATITUDE Consult™
• Version Model Number: 6294
• Company DUNS: 106295384
• 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: true
• Serial Number: false
• Manufacturing Date: false
• 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	00802526562907 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Approval: P910077

FDA Product Code

• OSR: Pacemaker/icd/crt non-implanted components

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: 2014-09-24

On-Brand Devices [LATITUDE Consult™]

• 00802526572722: LATITUDE Consult™ Communicator
• 00802526562914: LATITUDE Consult™ System
• 00802526562907: LATITUDE Consult™ System
• 00802526553516: LATITUDE Consult™ Communicator