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EasyMax Blood Glucose Test Strip

FDA UDI

Class II (US FDA UDI)

by Eps Bio Technology Corp.

Identity

Trade Name
EasyMax Blood Glucose Test Strip FDA UDI
Generic Name
Glucose IVD, kit, electrometry FDA UDI
Device Name
10 strips in a vial FDA UDI
Model / Reference
EasyMax FDA UDI
Description
10 strips in a vial FDA UDI

Identifiers

Primary DI / UDI-DI
00885017000355 FDA UDI
510(k) Number
K082121 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Glucose IVD, kit, electrometry

EasyMax Blood Glucose Test Strip by Eps Bio Technology Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Glucose IVD, kit, electrometry.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI f0801c40-f863-4814-a850-c2c748040eb6 36 fields · synced May 30, 2026