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MODD1 Infusion Set, 10 Pack

FDA UDI

Class II (US FDA UDI)

by Modular Medical, Inc.

Identity

Trade Name
MODD1 Infusion Set, 10 Pack FDA UDI
Generic Name
Electric infusion pump administration set, single-use FDA UDI
Device Name
Box of ten (10) MODD1 Infusion Sets FDA UDI
Model / Reference
MODD1 Insulin Delivery System FDA UDI
Description
Box of ten (10) MODD1 Infusion Sets FDA UDI

Identifiers

Catalog Number
MTL-67 FDA UDI
Primary DI / UDI-DI
00850037806041 FDA UDI
510(k) Number
K240158 FDA UDI
FDA Product Code
LZG FDA UDI
GMDN Term
Electric infusion pump administration set, single-use 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

Yes

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Electric infusion pump administration set, single-use

MODD1 Infusion Set, 10 Pack by Modular Medical, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Electric infusion pump administration set, single-use.

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 9256f5ec-8827-4548-8c64-dca8fb9886e0 37 fields · synced May 29, 2026