Identity
- Trade Name
- ARK™ Efavirenz Control FDA UDI
- Generic Name
- Multiple-therapy therapeutic drug monitoring IVD, kit, enzyme immunoassay (EIA) FDA UDI
- Device Name
- ARK™Efavirenz Control is intended for use in quality control of the ARK™Efavirenz Assay. FDA UDI
- Model / Reference
- 5017-0003-00 FDA UDI
- Description
- ARK™Efavirenz Control is intended for use in quality control of the ARK™Efavirenz Assay. FDA UDI
Identifiers
- Catalog Number
- 5017-0003-00 FDA UDI
- Primary DI / UDI-DI
- 00858724003384 FDA UDI
- GMDN Term
- Multiple-therapy therapeutic drug monitoring IVD, kit, enzyme immunoassay (EIA) FDA UDI
Classification
- 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-therapy therapeutic drug monitoring IVD, kit, enzyme immunoassay (EIA)
ARK™ Efavirenz Control by Ark Diagnostics Inc — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Multiple-therapy therapeutic drug monitoring IVD, kit, enzyme immunoassay (EIA).
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 | N/A | Pending data |
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Manufacturer
- Manufacturer
- Ark Diagnostics Inc
Sources (1)
- FDA UDI f0c727b8-c896-4884-918b-73386063e49c 36 fields · synced May 31, 2026