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Paradigm Real-Time Revel Insulin Pump With Enlite Sensor System

FDA UDI

Class III (US FDA UDI)

by Medtronic Minimed, Inc.

Identity

Trade Name
Paradigm Real-Time Revel Insulin Pump With Enlite Sensor System FDA UDI
Generic Name
Ambulatory insulin infusion pump, electronic, non-software-dosing FDA UDI
Device Name
PUMP MMT-723NAS PRDGM V3.0 SK US PR FDA UDI
Model / Reference
MMT-723NAS FDA UDI
Description
PUMP MMT-723NAS PRDGM V3.0 SK US PR FDA UDI

Identifiers

Primary DI / UDI-DI
00643169693814 FDA UDI
PMA Number
P150019 FDA UDI
P980022 FDA UDI
FDA Product Code
MDS FDA UDI
GMDN Term
Ambulatory insulin infusion pump, electronic, non-software-dosing FDA UDI

Classification

Device Class
Class III 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

Paradigm Real-Time Revel Insulin Pump With Enlite Sensor System by Medtronic Minimed, Inc. — Class III — FDA UDI — listed in FDA GUDID

Similar devices

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

Cleared under the same submission

P150019 also covers:

P980022 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 a26e6cae-9a20-4cde-b2c3-f1a93863c16c 36 fields · synced May 30, 2026