HVAD® Pump Implant Kit 1103

GUDID 00888707002639

Heartware Inc.

Implantable ventricular circulatory assist system

• Primary Device ID: 00888707002639
• NIH Device Record Key: 6f7e866b-258e-44d1-acbf-0d93b8bc7bd2
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: HVAD® Pump Implant Kit
• Version Model Number: 1103
• Catalog Number: 1103
• Company DUNS: 146054536
• Company Name: Heartware Inc.
• 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: 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	00888707002639 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Approval: P100047

FDA Product Code

• DSQ: Ventricular (Assisst) Bypass

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2017-05-18

On-Brand Devices [HVAD® Pump Implant Kit]

• 00888707002639: 1103
• 00888707005364: MCS1705PU
• 00888707009041: MCS1705PU