Lilly Together

Basic Information

• Brand Name: Lilly Together
• Primary DI: 00300021175559
• Version / Model: MA9140 IOS (Version 12)
• Catalog Number: MA9140001AM
• Company Name: ELI LILLY AND COMPANY
• Labeler DUNS: 006421325
• Distribution Status: In Commercial Distribution
• Device Count in Pkg: 1
• Record Status: Published
• Publish Date: 2024-02-16
• Public Version: 1
• Public Version Date: 2024-02-26
• Public Version Status: New
• Public Device Record Key: c94dfd36-2e0a-4f92-a5c1-af5702634114

Device Description

Software as a medical device (SaMD) for some Lilly medicines which provides access to medication reminders and customer support services; Operates on Apple iOS devices

Device Characteristics

• Single Use: No
• Prescription Use (Rx): No
• Over the Counter (OTC): Yes
• Kit: No
• Combination Product: No
• HCT/P: No
• Contains NRL: No
• Not Made with NRL: No
• MRI Safety: Labeling does not contain MRI Safety Information
• Direct Marking Exempt: No
• PM Exempt: Yes
• Has Serial Number: No
• Has Lot/Batch Number: Yes
• Has Manufacturing Date: No
• Has Expiration Date: No
• Has Donation ID: No

Sterilization

• Is Sterile: No
• Sterilization Prior Use: No

Product Codes

Code	Name	Medical Specialty	Regulation #	Device Class
NXQ	Reminder, Medication	Physical Medicine	890.5050	1
LMD	System, Digital Image Communications, Radiological	Radiology	892.2020	1

GMDN Terms

Code	Name	Definition	Implantable	Status
43081	Medication reminder application software	An individual software program or group of programs, routines and/or algorithms, that are used together with a mobile phone (cell phone) or other communication device to function as a medication reminder. It is intended for medical purposes to provide alerts to patients and healthcare providers for predetermined medication dosing schedules. It may also enable the delivery of information about medications, such as indications for use, dosing, side effects, and even photographs of different pills.	No	Active
64527	Patient subjective symptom recorder	A hand-held electrically-powered device designed for a patient to record the timing and/or severity of subjective symptoms, feelings, moods, and/or behaviours, typically by squeezing the device or pressing a push-button. It may have an internal memory for recording events and/or may wirelessly transmit to a smartphone app for recording or relaying to a central recording location. This is a reusable device.	No	Active

Identifiers

Type	ID	Issuing Agency	Package Type	Qty per Pkg	Pkg Status	Pkg Discontinue Date
Primary	00300021175559	GS1

Customer Contacts

• Phone: [phone]
• Email: [email protected]