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FreeStyle Libre Pro

FDA UDI

Class III (US FDA UDI)

by Abbott Diabetes Care Inc

Identity

Trade Name
FreeStyle Libre Pro FDA UDI
Generic Name
Percutaneous interstitial fluid glucose monitoring system, electrochemical FDA UDI
Device Name
FreeStyle Libre Pro Reader Kit US DOD FDA UDI
Model / Reference
71760 FDA UDI
Description
FreeStyle Libre Pro Reader Kit US DOD FDA UDI

Identifiers

Catalog Number
71760 FDA UDI
Primary DI / UDI-DI
00357599000417 FDA UDI
FDA Product Code
MDS FDA UDI
GMDN Term
Percutaneous interstitial fluid glucose monitoring system, electrochemical 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

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Percutaneous interstitial fluid glucose monitoring system, electrochemical

FreeStyle Libre Pro by Abbott Diabetes Care Inc — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

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

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Abbott Diabetes Care Inc

Sources (1)

  • FDA UDI f0fd8b1f-cb51-4953-bed7-87ea8ba00f30 36 fields · synced May 30, 2026