INVIVE™

GUDID 00802526536625

Cardiac Resynchronization Therapy Pacemaker

BOSTON SCIENTIFIC CORPORATION

Cardiac pulse generator test magnet

• Primary Device ID: 00802526536625
• NIH Device Record Key: 03bd79ea-812f-4352-a899-df6151f95c24
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: INVIVE™
• Version Model Number: V172
• 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: true
• Lot Batch: false
• Serial Number: true
• Manufacturing Date: false
• 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	00802526536625 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Approval: P030005

FDA Product Code

• NKE: Pulse generator, pacemaker, implantable, with cardiac resynchronization (CRT-P)

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2018-12-11
• Device Publish Date: 2014-09-24

On-Brand Devices [INVIVE™]

• 00802526536632: Cardiac Resynchronization Therapy Pacemaker
• 00802526536625: Cardiac Resynchronization Therapy Pacemaker