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Kroger Healthpro

FDA UDI

Class I (US FDA UDI)

by MHC Medical Products

Identity

Trade Name
Kroger Healthpro FDA UDI
Generic Name
Blood glucose/blood pressure monitoring system, home-use FDA UDI
Device Name
Kroger Blood Glucose Control Solution FDA UDI
Model / Reference
909011 FDA UDI
Description
Kroger Blood Glucose Control Solution FDA UDI

Identifiers

Catalog Number
909011 FDA UDI
Primary DI / UDI-DI
MHC19090112 FDA UDI
FDA Product Code
JJX FDA UDI
GMDN Term
Blood glucose/blood pressure monitoring system, home-use 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

Yes

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

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Blood glucose/blood pressure monitoring system, home-use

Kroger Healthpro by MHC Medical Products — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Blood glucose/blood pressure monitoring system, home-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI f60354c4-5132-4f26-83db-a121ccec0cac 34 fields · synced May 30, 2026