LATITUDE® Communicator with Wand

GUDID 00802526580727

LATITUDE ® Communicator with Wand

BOSTON SCIENTIFIC CORPORATION

Patient monitoring modem

• Primary Device ID: 00802526580727
• NIH Device Record Key: b5ef80e7-c3bd-47d9-8cec-65a6f4d352c4
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: LATITUDE® Communicator with Wand
• Version Model Number: 6481
• 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	00802526580727 [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: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2015-11-04

On-Brand Devices [LATITUDE® Communicator with Wand]

• 00802526580727: LATITUDE ® Communicator with Wand
• 00802526480485: LATITUDE ® Communicator with Wand