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MODD1 Starter Kit

FDA UDI

Class II (US FDA UDI)

by Modular Medical, Inc.

Identity

Trade Name
MODD1 Starter Kit FDA UDI
Generic Name
Ambulatory insulin infusion pump, electronic, non-software-dosing FDA UDI
Device Name
Kit containing one (1) of each of the following: Pump (software version v1.X), Infusion Set Inserter, User Guide, Quick Start Guide, and Patient Medical Device Card. FDA UDI
Model / Reference
MODD1 Insulin Delivery System FDA UDI
Description
Kit containing one (1) of each of the following: Pump (software version v1.X), Infusion Set Inserter, User Guide, Quick Start Guide, and Patient Medical Device Card. FDA UDI

Identifiers

Catalog Number
MTL-68 FDA UDI
Primary DI / UDI-DI
00850037806119 FDA UDI
510(k) Number
K163400 FDA UDI
K240158 FDA UDI
FDA Product Code
LZG FDA UDI
KZH FDA UDI
GMDN Term
Ambulatory insulin infusion pump, electronic, non-software-dosing FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5725 FDA UDI
880.6920 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

Yes

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Ambulatory insulin infusion pump, electronic, non-software-dosingInsulin infusion cannula introducer

MODD1 Starter Kit by Modular Medical, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Insulin infusion cannula introducer.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 444c5f03-e084-42d3-a719-f529abf8d960 37 fields · synced May 31, 2026