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Lilly Together

FDA UDI

Class I (US FDA UDI)

by Eli Lilly And Company

Identity

Trade Name
Lilly Together FDA UDI
Generic Name
Medication reminder application software FDA UDI
Device Name
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 FDA UDI
Model / Reference
MA9160 IOS (Version 14) FDA UDI
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 FDA UDI

Identifiers

Catalog Number
MA9160001AM FDA UDI
Primary DI / UDI-DI
00300021284558 FDA UDI
FDA Product Code
LMD FDA UDI
NXQ FDA UDI
GMDN Term
Medication reminder application software FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
892.2020 FDA UDI
890.5050 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

Yes

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Medication reminder application softwarePatient subjective symptom recorder

Lilly Together by Eli Lilly And Company — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Patient subjective symptom recorder.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Eli Lilly And Company

Sources (1)

  • FDA UDI c27c8ac2-e741-45d7-9f5a-1b51c0be8f53 35 fields · synced Jun 8, 2026