Identity
- Trade Name
- DOA FDA UDI
- Generic Name
- Multiple drugs of abuse IVD, kit, multiplex FDA UDI
- Device Name
- The Evidence® Drugs of Abuse (DOA) Assays are in-vitro diagnostic tests for the qualitative determination of the parent molecule and metabolites of drugs in human urine. They are competitive enzyme immunoassays. FDA UDI
- Model / Reference
- EV3542 FDA UDI
- Description
- The Evidence® Drugs of Abuse (DOA) Assays are in-vitro diagnostic tests for the qualitative determination of the parent molecule and metabolites of drugs in human urine. They are competitive enzyme immunoassays. FDA UDI
Identifiers
- Catalog Number
- EV3542 FDA UDI
- Primary DI / UDI-DI
- 05055273202397 FDA UDI
- 510(k) Number
- K030360 FDA UDIK040350 FDA UDIK040570 FDA UDIK041142 FDA UDIK041143 FDA UDIK041144 FDA UDIK043071 FDA UDIK050179 FDA UDI
- FDA Product Code
- DIO FDA UDIDJR FDA UDIDKZ FDA UDIDIS FDA UDIJXM FDA UDILDJ FDA UDIDJG FDA UDILCM FDA UDI
- GMDN Term
- Multiple drugs of abuse IVD, kit, multiplex FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 862.3250 FDA UDI862.3620 FDA UDI862.3100 FDA UDI862.3150 FDA UDI862.3170 FDA UDI862.3870 FDA UDI862.3650 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: Multiple drugs of abuse IVD, kit, multiplex
Doa by Randox Laboratories, Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Multiple drugs of abuse IVD, kit, multiplex.
Cleared under the same submission
K030360 also covers:
K040350 also covers:
K040570 also covers:
K041142 also covers:
K041143 also covers:
K041144 also covers:
K043071 also covers:
K050179 also covers:
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
- Randox Laboratories, Ltd.
Sources (1)
- FDA UDI b5360c00-28b5-4f5b-8502-ad70cb855f82 37 fields · synced May 30, 2026