HeartWare® Battery 1650DE

GUDID 00888707009942

Heartware Inc.

Implantable ventricular circulatory assist system

• Primary Device ID: 00888707009942
• NIH Device Record Key: e5d437e7-50ef-44b8-84f9-1ba3fbc3734e
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: HeartWare® Battery
• Version Model Number: 1650DE
• Catalog Number: 1650DE
• Company DUNS: 146054536
• Company Name: Heartware Inc.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Unsafe
• 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	00888707009942 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Approval: P100047

FDA Product Code

• DSQ: Ventricular (Assist) Bypass

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2022-08-23
• Device Publish Date: 2022-08-15

On-Brand Devices [HeartWare® Battery]

• 00888707006873: 1650DE
• 00888707005708: 1650DE
• 00888707005692: 1650DE
• 00888707002646: 1650DE
• 00888707000376: 1650
• 00888707000369: 1650DE
• 00888707000079: 1650
• 00888707006897: 1650DE
• 00888707009942: 1650DE
• 00888707008778: 1650DE
• 00763000629717: 1650DE