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FortisCare Self-Monitoring Blood Glucose System

FDA UDI

Class II (US FDA UDI)

by Eps Bio Technology Corp.

Identity

Trade Name
FortisCare Self-Monitoring Blood Glucose System FDA UDI
Generic Name
Glucose monitoring system IVD, home-use FDA UDI
Device Name
1 blood glucose meter; 10 strips in a vial; level 2 control solution in a convenience kit FDA UDI
Model / Reference
EM66 FDA UDI
Description
1 blood glucose meter; 10 strips in a vial; level 2 control solution in a convenience kit FDA UDI

Identifiers

Primary DI / UDI-DI
00885017000461 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

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

Yes

FDA UDI

Convenience Kit

Yes

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

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

FortisCare Self-Monitoring Blood Glucose System by Eps Bio Technology Corp. — 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 ecef23a2-41e5-4546-8555-28363b93a42f 36 fields · synced May 30, 2026