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CURO L5 Glucose test strip

FDA UDI

Class II (US FDA UDI)

by OSANG HEALTHCARE Co., Ltd.

Identity

Trade Name
CURO L5 Glucose test strip FDA UDI
Generic Name
Glucose monitoring system IVD, home-use FDA UDI
Device Name
Glucose test strip(25T) FDA UDI
Model / Reference
ILM-0001A FDA UDI
Description
Glucose test strip(25T) FDA UDI

Identifiers

Catalog Number
INFSG001EF FDA UDI
Primary DI / UDI-DI
08809115904119 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
Not 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

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

CURO L5 Glucose test strip by OSANG HEALTHCARE Co., Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 8bc7a365-46f8-4c2c-9439-c37cec38d1cb 37 fields · synced May 30, 2026