ReliOn® micro Blood Glucose Monitoring System

FDA UDI

Class II (US FDA UDI)

by Walmart Stores

Identity

Trade Name: ReliOn® micro Blood Glucose Monitoring System FDA UDI
Generic Name: Glucose monitoring system IVD, home-use FDA UDI
Device Name: Portable Blood Glucose Meter FDA UDI
Model / Reference: 710020 FDA UDI
Description: Portable Blood Glucose Meter FDA UDI

Identifiers

Primary DI / UDI-DI: 30605388492280 FDA UDI
FDA Product Code: NBW FDA UDI
GMDN Term: Glucose monitoring system IVD, home-use FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 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

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

FDA UDI

Manufacturing Date

FDA UDI

Category: Glucose monitoring system IVD, home-use

ReliOn® micro Blood Glucose Monitoring System by Walmart Stores — Class II — 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 II	Pending data

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Manufacturer

Manufacturer: Walmart Stores

Sources (1)

FDA UDI 84041ae9-ffaa-470d-8df8-7b097927ada0 35 fields · synced May 31, 2026