Identity
- Trade Name
- Dimension® Flex® reagent cartridge AMPH FDA UDI
- Generic Name
- Amphetamine-specific IVD, kit, enzyme immunoassay (EIA) FDA UDI
- Device Name
- Urine Amphetamine/Methamphetamine Screen Flex® reagent cartridge, 80 tests FDA UDI
- Model / Reference
- 10444926 FDA UDI
- Description
- Urine Amphetamine/Methamphetamine Screen Flex® reagent cartridge, 80 tests FDA UDI
Identifiers
- Catalog Number
- DF91B FDA UDI
- Primary DI / UDI-DI
- 00842768005817 FDA UDI
- 510(k) Number
- K040133 FDA UDI
- FDA Product Code
- DKZ FDA UDI
- GMDN Term
- Amphetamine-specific IVD, kit, enzyme immunoassay (EIA) FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 862.3100 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
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: Amphetamine-specific IVD, kit, enzyme immunoassay (EIA)
Dimension® Flex® reagent cartridge AMPH by Siemens Healthcare Diagnostics — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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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 |
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Manufacturer
- Manufacturer
- Siemens Healthcare Diagnostics
Sources (1)
- FDA UDI f5509476-f8ad-42ab-9f9d-3cf4320b4b4d 37 fields · synced May 30, 2026