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Leader

FDA UDI

Class I (US FDA UDI)

by Cardinal Health 110, Inc.

Identity

Trade Name
LEADER FDA UDI
Generic Name
Glucose IVD, control FDA UDI
Device Name
LDR Glucose Control Solution 3x2mL solutions FDA UDI
Model / Reference
5277306 FDA UDI
Description
LDR Glucose Control Solution 3x2mL solutions FDA UDI

Identifiers

Catalog Number
5277306 FDA UDI
Primary DI / UDI-DI
00096295129182 FDA UDI
FDA Product Code
JJX FDA UDI
GMDN Term
Glucose IVD, control FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.1660 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

No

FDA UDI

Over-the-Counter

Yes

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Glucose IVD, control

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

Similar devices

Also classified as Glucose IVD, control.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 79a1a63c-6fdb-40d5-8631-1c19646b9940 36 fields · synced Jun 1, 2026