LATITUDE® Communicator

GUDID 00802526516115

LATITUDE ® Communicator

BOSTON SCIENTIFIC CORPORATION

Medical networking interface unit

• Primary Device ID: 00802526516115
• NIH Device Record Key: 043b5ba0-ed52-4af5-a861-5a571c6017d7
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: LATITUDE® Communicator
• Version Model Number: 6476
• 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: false
• Serial Number: true
• Manufacturing Date: true
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00802526516115 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Approval: P910077

FDA Product Code

• LWS: Implantable cardioverter defibrillator (non-CRT)

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: 2018-07-06
• Device Publish Date: 2014-09-24

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• 00802526570322: LATITUDE ® Communicator
• 00802526570209: LATITUDE ® Communicator
• 00802526554704: LATITUDE ® Communicator
• 00802526544224: LATITUDE ® Communicator
• 00802526544118: LATITUDE ® Communicator
• 00802526516146: LATITUDE ® Communicator
• 00802526516115: LATITUDE ® Communicator