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Alere iScreen Dx

FDA UDI

Class II (US FDA UDI)

by Instant Technologies, Inc.

Identity

Trade Name
Alere iScreen Dx FDA UDI
Generic Name
Amphetamine/methamphetamine group IVD, kit, rapid ICT, clinical FDA UDI
Device Name
Urine Drug Screen Card for detection of Ecstasy (MDMA) single drug, CLIA Waived FDA UDI
Model / Reference
IS1 MDM-DX FDA UDI
Description
Urine Drug Screen Card for detection of Ecstasy (MDMA) single drug, CLIA Waived FDA UDI

Identifiers

Catalog Number
IS1 MDM-DX FDA UDI
Primary DI / UDI-DI
00817405020096 FDA UDI
510(k) Number
K022355 FDA UDI
FDA Product Code
DJC FDA UDI
GMDN Term
Amphetamine/methamphetamine group IVD, kit, rapid ICT, clinical FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
862.3610 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

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

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, clinical

Alere iScreen Dx by Instant Technologies, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Amphetamine/methamphetamine group IVD, kit, rapid ICT, clinical.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI e5bc4428-10f1-4abd-a1e2-ae786c0be33e 37 fields · synced Jun 1, 2026