GUDIDData
gudid Primary ID: MA9141 Android (Version 17)

Lilly Together (UDI MA9141 Android (Version 17))

Manufactured by ELI LILLY AND COMPANY

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Lilly Together - Primary ID MA9141 Android (Version 17)

Device Regulatory Overview

The Lilly Together (Model/Catalog Number: MA9141 Android (Version 17)) is a medical device manufactured by ELI LILLY AND COMPANY. This product is indexed under FDA Product Code / Category Classification LMD within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
MA9141 Android (Version 17)
Product Code / EMDN
LMD
Device Name
Software as a medical device (SaMD) for some Lilly medicines which provides access to medication reminders and customer support services; Operates on Android devices (various manufacturers)
Database Sync Date
2026-08-09 09:20:17

Full Regulatory Attributes

🔒 Token Gated
{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}
                            

Unlock Compliance Data & Serialization Specs

Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.

Get API Token Access ($49/mo)

Frequently Asked Questions

Who is the primary manufacturer of Lilly Together?

The registered manufacturer of record for Lilly Together is ELI LILLY AND COMPANY.

What is the Primary UDI-DI identifier for Lilly Together?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is MA9141 Android (Version 17).

What classification code is assigned to this device?

This device is registered under product classification code LMD.

Programmatic Export

Export this master device record as standardized JSON or CSV for compliance audits.

JSON API Endpoint