HeartWare® Battery 1650

GUDID 00888707000079

Heartware Inc.

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• Primary Device ID: 00888707000079
• NIH Device Record Key: e3aaa351-4b4c-4fb0-bc1a-6d39d2cd3ae2
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: HeartWare® Battery
• Version Model Number: 1650
• Catalog Number: 1650
• 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	00888707000079 [Primary]

FDA Product Code

• DSQ: Ventricular (Assisst) Bypass

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2014-08-13

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