HumaPen® Luxura™ HD MS9673

GUDID 00300029673019

HumaPen Luxura HD is a reusable pen injector intended for use with Lilly 3 mL insulin cartridges.

ELI LILLY AND COMPANY

Cartridge-accepting autoinjector, mechanical Empty self-injector, mechanical Empty self-injector, mechanical Empty self-injector, mechanical Empty self-injector, mechanical Empty self-injector, mechanical Empty self-injector, mechanical Empty self-injector, mechanical Empty self-injector, mechanical Empty self-injector, mechanical Empty self-injector, mechanical Empty self-injector, mechanical Empty self-injector, mechanical Empty self-injector, mechanical Empty self-injector, mechanical

• Primary Device ID: 00300029673019
• NIH Device Record Key: 7c4a671a-8c83-4764-bf12-20c3e8f01451
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: HumaPen® Luxura™ HD
• Version Model Number: MS9673
• Catalog Number: MS9673
• Company DUNS: 006421325
• Company Name: ELI LILLY AND COMPANY
• 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: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: 1-800-545-5979
• Email: xxx@xxx.xxx
• Phone: 1-800-545-5979
• Email: xxx@xxx.xxx
• Phone: 1-800-545-5979
• Email: xxx@xxx.xxx
• Phone: 1-800-545-5979
• Email: xxx@xxx.xxx
• Phone: 1-800-545-5979
• Email: xxx@xxx.xxx
• Phone: 1-800-545-5979
• Email: xxx@xxx.xxx
• Phone: 1-800-545-5979
• Email: xxx@xxx.xxx
• Phone: 1-800-545-5979
• Email: xxx@xxx.xxx
• Phone: 1-800-545-5979
• Email: xxx@xxx.xxx
• Phone: 1-800-545-5979
• Email: xxx@xxx.xxx
• Phone: 1-800-545-5979
• Email: xxx@xxx.xxx
• Phone: 1-800-545-5979
• Email: xxx@xxx.xxx
• Phone: 1-800-545-5979
• Email: xxx@xxx.xxx
• Phone: 1-800-545-5979
• Email: xxx@xxx.xxx
• Phone: 1-800-545-5979
• Email: xxx@xxx.xxx

Device Identifiers

Device Issuing Agency	Device ID
GS1	00300029673019 [Primary]
GS1	30300029673010 [Package]; Package: Case [25 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K100988

FDA Product Code

• FMF: Syringe, Piston

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: 2016-09-21

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