← Back to catalogue

Tandem Mobi Cartridge

FDA UDI

Class II (US FDA UDI)

by Tandem Diabetes Care, Inc.

Identity

Trade Name
Tandem Mobi Cartridge FDA UDI
Generic Name
Ambulatory insulin infusion pump reservoir FDA UDI
Device Name
Tandem Mobi Cartridge, 2 Pack FDA UDI
Model / Reference
1013754 FDA UDI
Description
Tandem Mobi Cartridge, 2 Pack FDA UDI

Identifiers

Primary DI / UDI-DI
00389152375458 FDA UDI
510(k) Number
K223213 FDA UDI
FDA Product Code
QFG FDA UDI
GMDN Term
Ambulatory insulin infusion pump reservoir FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5730 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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Ambulatory insulin infusion pump reservoir

Tandem Mobi Cartridge by Tandem Diabetes Care, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ambulatory insulin infusion pump reservoir.

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 4afdfb93-9f44-4521-bd40-e9956858e3ee 34 fields · synced Jun 8, 2026