Leader

FDA UDI

Class I (US FDA UDI)

by Cardinal Health 110, Inc.

Identity

Trade Name: LEADER FDA UDI
Generic Name: Glucose monitoring system IVD, home-use FDA UDI
Device Name: LDR Blood Glucose Monitoring System FDA UDI
Model / Reference: 5277181 FDA UDI
Description: LDR Blood Glucose Monitoring System FDA UDI

Identifiers

Catalog Number: 5277181 FDA UDI
Primary DI / UDI-DI: 00096295129144 FDA UDI
FDA Product Code: JJX FDA UDI
NBW FDA UDI
CGA FDA UDI
GMDN Term: Glucose monitoring system IVD, home-use FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 862.1660 FDA UDI
862.1345 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

Yes

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Glucose monitoring system IVD, home-use

Leader by Cardinal Health 110, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Cardinal Health 110, Inc.

Sources (1)

FDA UDI 76daa468-c29e-4b4f-ade7-a377ef6cf88c 36 fields · synced May 30, 2026