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Single Panel Pre Screen Plus Dip Card

FDA UDI

Class II (US FDA UDI)

by Mergers Marketing, Inc.

Identity

Trade Name
Single Panel Pre Screen Plus Dip Card FDA UDI
Generic Name
Multiple drugs of abuse IVD, kit, rapid ICT, clinical FDA UDI
Device Name
Single Panel Pre Screen Plus Dip Card Drug Combo: ETG FDA UDI
Model / Reference
PS-ETG FDA UDI
Description
Single Panel Pre Screen Plus Dip Card Drug Combo: ETG FDA UDI

Identifiers

Primary DI / UDI-DI
00851000007083 FDA UDI
FDA Product Code
DOJ FDA UDI
GMDN Term
Multiple drugs of abuse IVD, kit, rapid ICT, clinical FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
862.3040 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

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

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: Multiple drugs of abuse IVD, kit, rapid ICT, clinical

Single Panel Pre Screen Plus Dip Card by Mergers Marketing, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Multiple drugs of abuse IVD, kit, rapid ICT, clinical.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 614b091e-dc01-4e3a-8271-2a323b3fdad5 33 fields · synced May 30, 2026