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Greater Goods

FDA UDI

Class II (US FDA UDI)

by Greater Goods, LLC

Identity

Trade Name
Greater Goods FDA UDI
Generic Name
Blood glucose/blood pressure monitoring system, home-use FDA UDI
Device Name
0031 Cellular BGM FDA UDI
Model / Reference
0031 FDA UDI
Description
0031 Cellular BGM FDA UDI

Identifiers

Primary DI / UDI-DI
00875011000314 FDA UDI
510(k) Number
K223722 FDA UDI
FDA Product Code
NBW FDA UDI
GMDN Term
Blood glucose/blood pressure monitoring system, 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

Yes

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

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

Greater Goods by Greater Goods, LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

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

Cleared under the same submission

K223722 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Greater Goods, LLC

Sources (1)

  • FDA UDI 34808545-a6f7-4d73-8c95-b03859557a6c 34 fields · synced May 30, 2026