LATITUDE® Communicator

GUDID 00802526577307

LATITUDE ® Communicator

BOSTON SCIENTIFIC CORPORATION

Medical networking interface unit

• Primary Device ID: 00802526577307
• NIH Device Record Key: a43f705c-9f0f-4f1c-8bbf-3c6b1f9767b1
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: LATITUDE® Communicator
• Version Model Number: 6280
• 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: 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	00802526577307 [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: 6
• Public Version Date: 2019-10-28
• Device Publish Date: 2015-11-04

On-Brand Devices [LATITUDE® Communicator]

• 00802526585609: LATITUDE ™ Communicator
• 00802526580802: LATITUDE ® Communicator
• 00802526577451: LATITUDE ® Communicator
• 00802526577307: LATITUDE ® Communicator
• 00802526570322: LATITUDE ® Communicator
• 00802526570209: LATITUDE ® Communicator
• 00802526554704: LATITUDE ® Communicator
• 00802526544224: LATITUDE ® Communicator
• 00802526544118: LATITUDE ® Communicator
• 00802526516146: LATITUDE ® Communicator
• 00802526516115: LATITUDE ® Communicator