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
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Cleared under the same submission
K022355 also covers:
- CLIAwaived — CLIAWAIVED,INC.
- CLIAwaived — CLIAWAIVED,INC.
- CLIAwaived — CLIAWAIVED,INC.
- CLIAwaived — CLIAWAIVED,INC.
- CLIAwaived — CLIAWAIVED,INC.
- CLIAwaived — CLIAWAIVED,INC.
- CLIAwaived — CLIAWAIVED,INC.
- Alere iScreen Dx — Instant Technologies, Inc.
- Alere iScreen Dx — Instant Technologies, Inc.
- Alere iScreen Dx — Instant Technologies, Inc.
- Alere iScreen Dx — Instant Technologies, Inc.
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Instant Technologies, Inc.
Sources (1)
- FDA UDI e5bc4428-10f1-4abd-a1e2-ae786c0be33e 37 fields · synced Jun 1, 2026