MiniMed™ Mobile

FDA UDI

Class II (US FDA UDI)

by Medtronic Minimed, Inc.

Identity

Trade Name: MiniMed™ Mobile FDA UDI
Generic Name: Self-care monitoring/reporting software FDA UDI
Device Name: Sftwr MMT-6102 AHCL 2.1.1 App iOS FDA UDI
Model / Reference: MMT-6102 FDA UDI
Description: Sftwr MMT-6102 AHCL 2.1.1 App iOS FDA UDI

Identifiers

Primary DI / UDI-DI: 00763000827793 FDA UDI
FDA Product Code: PJT FDA UDI
PKU FDA UDI
GMDN Term: Self-care monitoring/reporting software FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 862.1350 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Category: Self-care monitoring/reporting software

MiniMed™ Mobile by Medtronic Minimed, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Medtronic Minimed, Inc.

Sources (1)

FDA UDI 0c741834-106b-4876-8234-0ab21c08d4fe 34 fields · synced May 30, 2026