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MiniMed ® Connect

FDA UDI

Class II (US FDA UDI)

by Medtronic Minimed, Inc.

Identity

Trade Name
MiniMed ® Connect FDA UDI
Generic Name
Ambulatory insulin infusion pump, electronic, non-software-dosing FDA UDI
Device Name
KIT MMT-7000NAU PRDGM XMTR CONN BT US FDA UDI
Model / Reference
MMT-7000NAU FDA UDI
Description
KIT MMT-7000NAU PRDGM XMTR CONN BT US FDA UDI

Identifiers

Primary DI / UDI-DI
00643169873827 FDA UDI
510(k) Number
K151236 FDA UDI
FDA Product Code
PKU FDA UDI
GMDN Term
Ambulatory insulin infusion pump, electronic, non-software-dosing 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

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

No

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Ambulatory insulin infusion pump, electronic, non-software-dosing

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

Similar devices

Also classified as Ambulatory insulin infusion pump, electronic, non-software-dosing.

Cleared under the same submission

K151236 also covers:

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 fa63eb63-99f8-4ea5-b050-555c12881f4f 36 fields · synced Jun 7, 2026