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VivaGuard Ino Smart Blood Glucose Meter

FDA UDI

Class II (US FDA UDI)

by ABOUND Diagnostics, Inc

Identity

Trade Name
VivaGuard Ino Smart Blood Glucose Meter FDA UDI
Generic Name
Glucose analyser IVD, home-use FDA UDI
Device Name
VivaGuard Ino Smart Blood Glucose Meter FDA UDI
Model / Reference
VGM04-665 FDA UDI
Description
VivaGuard Ino Smart Blood Glucose Meter FDA UDI

Identifiers

Catalog Number
VGM04-665 FDA UDI
Primary DI / UDI-DI
00840423500059 FDA UDI
FDA Product Code
NBW FDA UDI
CGA FDA UDI
JJX FDA UDI
GMDN Term
Glucose analyser IVD, home-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
862.1345 FDA UDI
862.1660 FDA UDI
Commercial Distribution
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

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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Glucose analyser IVD, home-use

VivaGuard Ino Smart Blood Glucose Meter by ABOUND Diagnostics, Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Glucose analyser IVD, home-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI f4363a45-3b50-4d3b-a687-870ceb05b821 34 fields · synced May 31, 2026