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Equate

FDA UDI

Class II (US FDA UDI)

by Walmart Stores

Identity

Trade Name
Equate FDA UDI
Generic Name
Opiate/opiate metabolite IVD, reagent FDA UDI
Device Name
EQ 12 PANEL DRG TEST FDA UDI
Model / Reference
572627460 FDA UDI
Description
EQ 12 PANEL DRG TEST FDA UDI

Identifiers

Primary DI / UDI-DI
00681131089869 FDA UDI
FDA Product Code
NFT FDA UDI
PTH FDA UDI
NFV FDA UDI
NFY FDA UDI
NGG FDA UDI
PTG FDA UDI
NGL FDA UDI
NGM FDA UDI
QAW FDA UDI
NFW FDA UDI
GMDN Term
Opiate/opiate metabolite IVD, reagent FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
862.3100 FDA UDI
862.3150 FDA UDI
862.3170 FDA UDI
862.3250 FDA UDI
862.3610 FDA UDI
862.3620 FDA UDI
862.3650 FDA UDI
862.3910 FDA UDI
862.3870 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: Barbiturate IVD, kit, rapid ICT, clinicalAmphetamine/methamphetamine group IVD, kit, rapid ICT, clinicalCannabinoid/cannabinoid metabolite IVD, reagentCocaine/cocaine metabolite IVD, reagent

Equate by Walmart Stores — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Nortriptyline IVD, reagent.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Walmart Stores

Sources (1)

  • FDA UDI a942917f-164c-42fc-aaa1-25591eb9b353 33 fields · synced Jun 1, 2026