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OKRA Glucose Test Strip Refill kit

FDA UDI

Class II (US FDA UDI)

by OSANG HEALTHCARE Co., Ltd.

Identity

Trade Name
OKRA Glucose Test Strip Refill kit FDA UDI
Generic Name
Glucose IVD, kit, electrometry FDA UDI
Device Name
Blood Glucose Test strips Refill kit FDA UDI
Model / Reference
IGM-1003A FDA UDI
Description
Blood Glucose Test strips Refill kit FDA UDI

Identifiers

Primary DI / UDI-DI
08809115905697 FDA UDI
FDA Product Code
NBW FDA UDI
GMDN Term
Glucose IVD, kit, electrometry 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

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Glucose IVD, kit, electrometry

OKRA Glucose Test Strip Refill kit by OSANG HEALTHCARE Co., Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Glucose IVD, kit, electrometry.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 48b072f6-49cf-49f0-a272-139c1406523c 35 fields · synced May 30, 2026