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Non-Esterified Fatty Acids (NEFA)

FDA UDI

Class I (US FDA UDI)

by Randox Laboratories, Ltd.

Identity

Trade Name
Non-Esterified Fatty Acids (NEFA) FDA UDI
Generic Name
Non-esterified fatty acid IVD, kit, enzyme immunoassay (EIA) FDA UDI
Model / Reference
FA115 FDA UDI

Identifiers

Primary DI / UDI-DI
05055273203066 FDA UDI
FDA Product Code
JLG FDA UDI
GMDN Term
Non-esterified fatty acid IVD, kit, enzyme immunoassay (EIA) FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.1290 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

No

FDA UDI

Convenience Kit

Yes

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: Non-esterified fatty acid IVD, kit, enzyme immunoassay (EIA)

Non-Esterified Fatty Acids (NEFA) by Randox Laboratories, Ltd. — Class I — 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 882d105a-d910-4f1b-b08e-8c7d00db26c4 32 fields · synced May 30, 2026