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VeriQuick

FDA UDI

Class II (US FDA UDI)

by Fourstar Group Inc.

Identity

Trade Name
VeriQuick FDA UDI
Generic Name
Moist-heat pack FDA UDI
Device Name
At Home Marijuana Drug Test FDA UDI
Model / Reference
11012637B FDA UDI
Description
At Home Marijuana Drug Test FDA UDI

Identifiers

Primary DI / UDI-DI
00049696712675 FDA UDI
FDA Product Code
LDJ FDA UDI
GMDN Term
Moist-heat pack FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
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

No

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: Moist-heat pack

VeriQuick by Fourstar Group Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Moist-heat pack.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Fourstar Group Inc.

Sources (1)

  • FDA UDI 60420f7e-d7c6-4227-9080-2febf15fbf41 33 fields · synced May 31, 2026