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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
Percutaneous interstitial fluid glucose monitoring system, electrochemical FDA UDI
Device Name
KIT MMT-7000NA PRDGM XMTR CONN BT US FDA UDI
Model / Reference
MMT-7000NA FDA UDI
Description
KIT MMT-7000NA PRDGM XMTR CONN BT US FDA UDI

Identifiers

Primary DI / UDI-DI
00643169631373 FDA UDI
510(k) Number
K151236 FDA UDI
FDA Product Code
PKU FDA UDI
GMDN Term
Percutaneous interstitial fluid glucose monitoring system, electrochemical 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

Yes

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

Category: Percutaneous interstitial fluid glucose monitoring system, electrochemical

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

Similar devices

Also classified as Percutaneous interstitial fluid glucose monitoring system, electrochemical.

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 ccf02191-ddec-4100-8982-b428fae95db3 36 fields · synced May 30, 2026