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Fora

FDA UDI

Class I (US FDA UDI)

by Fora Care Inc.

Identity

Trade Name
FORA FDA UDI
Generic Name
Ketone (acetoacetate) IVD, reagent FDA UDI
Device Name
Blood Ketone Test Strip FDA UDI
Model / Reference
GTel/Test N'GO Advance/Test N'GO Advance Voice/Test N'GO Adv. Mobile FDA UDI
Description
Blood Ketone Test Strip FDA UDI

Identifiers

Primary DI / UDI-DI
00816042015076 FDA UDI
FDA Product Code
JIN FDA UDI
GMDN Term
Ketone (acetoacetate) IVD, reagent FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.1435 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: Ketone (acetoacetate) IVD, reagent

Fora by Fora Care Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ketone (acetoacetate) IVD, reagent.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Fora Care Inc.

Sources (1)

  • FDA UDI 4e98af3e-a2eb-49b7-9532-81c84d9d27f3 33 fields · synced May 30, 2026