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Walgreens

FDA UDI

Class II (US FDA UDI)

by Walgreen Co.

Identity

Trade Name
Walgreens FDA UDI
Generic Name
Cannabinoid/cannabinoid metabolite IVD, reagent FDA UDI
Device Name
7 Drugs Tested Home Drug Test - AMP1000COC300/MDMA500/MET1000/OPI2000/PCP25/THC50 FDA UDI
Model / Reference
765430 FDA UDI
Description
7 Drugs Tested Home Drug Test - AMP1000COC300/MDMA500/MET1000/OPI2000/PCP25/THC50 FDA UDI

Identifiers

Primary DI / UDI-DI
00311917034218 FDA UDI
FDA Product Code
NFW FDA UDI
NFY FDA UDI
NGG FDA UDI
NGL FDA UDI
NGM FDA UDI
NFT FDA UDI
GMDN Term
Cannabinoid/cannabinoid metabolite IVD, reagent FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
862.3870 FDA UDI
862.3250 FDA UDI
862.3610 FDA UDI
862.3650 FDA UDI
862.3100 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: Amphetamine/methamphetamine group IVD, kit, rapid ICT, clinicalCannabinoid/cannabinoid metabolite IVD, reagentCocaine/cocaine metabolite IVD, reagentOpiate/opiate metabolite IVD, reagent

Walgreens by Walgreen Co. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Phencyclidine (PCP) IVD, reagent.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Walgreen Co.

Sources (1)

  • FDA UDI d63e01bf-d773-4816-93df-fd38508665cb 34 fields · synced Jun 7, 2026