CURO G6s Smart Glucose Meter

FDA UDI

Class II (US FDA UDI)

by Kpi Healthcare, Inc.

Identity

Trade Name: CURO G6s Smart Glucose Meter FDA UDI
Generic Name: Ambulatory insulin infusion pump/interstitial glucose monitoring system FDA UDI
Device Name: CURO G6s Smart Glucose Meter FDA UDI
Model / Reference: CURO G6s Smart Glucose Meter FDA UDI
Description: CURO G6s Smart Glucose Meter FDA UDI

Identifiers

Primary DI / UDI-DI: 00860394001249 FDA UDI
FDA Product Code: NBW FDA UDI
GMDN Term: Ambulatory insulin infusion pump/interstitial glucose monitoring system 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

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

Yes

FDA UDI

Category: Glucose monitoring system IVD, home-use Glucose monitoring system IVD, point-of-care Blood glucose/blood pressure monitoring system, home-use Glucose analyser IVD, home-use

CURO G6s Smart Glucose Meter by Kpi Healthcare, Inc. — 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: Kpi Healthcare, Inc.

Sources (1)

FDA UDI 88379c73-9693-4c7d-ab2e-ccec4a617aba 33 fields · synced May 30, 2026