← Back to catalogue

MMI App for iOS

FDA UDI

Class II (US FDA UDI)

by Modular Medical, Inc.

Identity

Trade Name
MMI App for iOS FDA UDI
Generic Name
Ambulatory insulin infusion pump software, patient-dosing FDA UDI
Device Name
iOS smartphone application for MODD1 Insulin Delivery System, software version v1.X FDA UDI
Model / Reference
MODD1 Insulin Delivery System FDA UDI
Description
iOS smartphone application for MODD1 Insulin Delivery System, software version v1.X FDA UDI

Identifiers

Catalog Number
MTL-103 FDA UDI
Primary DI / UDI-DI
00850037806010 FDA UDI
510(k) Number
K240158 FDA UDI
FDA Product Code
LZG FDA UDI
GMDN Term
Ambulatory insulin infusion pump software, patient-dosing FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5725 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

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Ambulatory insulin infusion pump software, patient-dosing

MMI App for iOS by Modular Medical, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 08550141-8740-4dd4-91b0-e486f3a077ce 36 fields · synced May 30, 2026