← Back to catalogue

Meijer Essential Wireless Blood Glucose Meter

FDA UDI

Class II (US FDA UDI)

by Meijer, Inc.

Identity

Trade Name
Meijer Essential Wireless Blood Glucose Meter FDA UDI
Generic Name
Glucose monitoring system IVD, home-use FDA UDI
Device Name
Blood Glucose Meter, Meijer, Essential, Wireless FDA UDI
Model / Reference
8000-10845 FDA UDI
Description
Blood Glucose Meter, Meijer, Essential, Wireless FDA UDI

Identifiers

Primary DI / UDI-DI
10760236150364 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

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

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

Category: Glucose monitoring system IVD, home-use

Meijer Essential Wireless Blood Glucose Meter by Meijer, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Glucose monitoring system IVD, home-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Meijer, Inc.

Sources (1)

  • FDA UDI f421d8be-a111-4a80-9f54-b0fa37c33b12 33 fields · synced May 30, 2026