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CareLink™ Connect

FDA UDI

Class II (US FDA UDI)

by Medtronic Minimed, Inc.

Identity

Trade Name
CareLink™ Connect FDA UDI
Generic Name
Patient health record information system application software FDA UDI
Device Name
SFTWR MMT-6112 CP IOS V2.3.0 US FDA UDI
Model / Reference
MMT-6112 FDA UDI
Description
SFTWR MMT-6112 CP IOS V2.3.0 US FDA UDI

Identifiers

Primary DI / UDI-DI
00763000437787 FDA UDI
FDA Product Code
PKU FDA UDI
GMDN Term
Patient health record information system application 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

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Patient health record information system application software

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

Similar devices

Also classified as Patient health record information system application software.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Medtronic Minimed, Inc.

Sources (1)

  • FDA UDI 96398a48-32d2-45a3-9fed-4aea340f40c7 34 fields · synced May 30, 2026