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ENLiTE™

FDA UDI

Class III (US FDA UDI)

by Medtronic Minimed, Inc.

Identity

Trade Name
ENLiTE™ FDA UDI
Generic Name
Percutaneous interstitial fluid glucose monitoring system sensor FDA UDI
Device Name
SENSOR MMT-7008B ENLITE NFIN 2L PLUS FDA UDI
Model / Reference
MMT-7008B FDA UDI
Description
SENSOR MMT-7008B ENLITE NFIN 2L PLUS FDA UDI

Identifiers

Primary DI / UDI-DI
00643169455535 FDA UDI
PMA Number
P150001 FDA UDI
FDA Product Code
OZO FDA UDI
GMDN Term
Percutaneous interstitial fluid glucose monitoring system sensor FDA UDI

Classification

Device Class
Class III FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Percutaneous interstitial fluid glucose monitoring system sensor

ENLiTE™ by Medtronic Minimed, Inc. — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Percutaneous interstitial fluid glucose monitoring system sensor.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 372ffaed-4379-437d-a158-46f8cb04bf81 36 fields · synced May 30, 2026