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DRI MDA Control

FDA UDI

Class I (US FDA UDI)

by Microgenics Corporation

Identity

Trade Name
DRI MDA Control FDA UDI
Generic Name
Amphetamine/methamphetamine group IVD, control FDA UDI
Model / Reference
10024435 FDA UDI

Identifiers

Primary DI / UDI-DI
00884883006843 FDA UDI
FDA Product Code
LAS FDA UDI
GMDN Term
Amphetamine/methamphetamine group IVD, control FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.3280 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

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: Amphetamine/methamphetamine group IVD, control

DRI MDA Control by Microgenics Corporation — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Amphetamine/methamphetamine group IVD, control.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 99e47409-5fb0-4f6b-982b-72dae8496c62 32 fields · synced Jun 9, 2026