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Fora

FDA UDI

Class I (US FDA UDI)

by Fora Care Inc.

Identity

Trade Name
FORA FDA UDI
Generic Name
Total cholesterol lipid IVD, calibrator FDA UDI
Device Name
For Total Cholesterol test FDA UDI
Model / Reference
Control Solution (L1) FDA UDI
Description
For Total Cholesterol test FDA UDI

Identifiers

Primary DI / UDI-DI
00816042014093 FDA UDI
FDA Product Code
JJX FDA UDI
GMDN Term
Total cholesterol lipid IVD, calibrator FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
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

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Total cholesterol lipid IVD, calibrator

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

Similar devices

Also classified as Total cholesterol lipid IVD, calibrator.

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 4bfa599d-7263-4044-9d16-5f77be75a9a6 33 fields · synced Jun 1, 2026