ARK™ Eddp Assay
The ARK EDDP Assay measures EDDP in human urine qualitatively or semiquantitatively at cutoffs of 100 and 300 ng/mL. It is a prescription laboratory immunoassay for compatible automated…
The ARK EDDP Assay measures EDDP in human urine qualitatively or semiquantitatively at cutoffs of 100 and 300 ng/mL. It is a prescription laboratory immunoassay for compatible automated clinical chemistry analyzers.
The two reagent system uses an anti-EDDP antibody and enzyme labeled EDDP derivative. Competition for antibody binding changes enzyme activity, creating an absorbance signal related to the concentration of EDDP in the specimen.
Listed Item
The ARK™ EDDP Assay is intended for the qualitative and/or semiquantitative determination of EDDP in human urine at cutoff concentrations of 100 ng/mL and 300 ng/mL. The assay provides a simple and rapid analytical screening procedure for detecting EDDP in urine and is designated for professional use on automated clinical chemistry analyzers.
Confirming Results
The result is preliminary and a positive result requires a more specific chemical confirmation method, such as GC/MS or LC-MS/MS. Semiquantitative results support selection of specimen dilution for confirmation and laboratory quality control procedures.
Who Else Makes It
Concentrated in Zhejiang (6), Guangdong (2), Beijing (1). 4 of them are registered as contract manufacturers, able to build to a buyer’s own specification.
| Manufacturer | City | Province | Registered as | Device types |
|---|---|---|---|---|
| Zhejiang Orient Gene Biotech | Huzhou | Zhejiang | Contract manufacturer | 86 |
| Hangzhou Biotest Biotech Co., Ltd. | Hangzhou | Zhejiang | Contract manufacturer | 41 |
| Abon Biopharm (Hangzhou) Co., Ltd. | Hangzhou | Zhejiang | Contract manufacturer | 17 |
| Prometheus Bio Inc. | Hangzhou | Zhejiang | Contract manufacturer | 12 |
| Hangzhou AllTest Biotech Co., Ltd. | Hangzhou | Zhejiang | Contract manufacturer | 48 |
| Assure Tech. (Hangzhou) Co., Ltd. | Hangzhou | Zhejiang | Contract manufacturer | 48 |
| W.h.p.m. Bioresearch & Technology Co., Ltd. | Beijing | Beijing | Manufacturer | 37 |
| Guangzhou Decheng Biotechnology Co., Ltd. | Guangzhou | Guangdong | Complaint-file establishment | 35 |
| Changchun Wancheng BIO-Electron Co., Ltd. | Changchun | Jilin | Contract manufacturer | 34 |
| Co-Innovation Biotech Co., Ltd. | Guangzhou | Guangdong | Contract manufacturer | 29 |
| Hongkong Conlight Medical Group Limited | Tai Kok Tsui | Hong Kong | Specification developer | 11 |
Record
| Listed by | ARK Diagnostics Inc, United States |
|---|---|
| FDA product code | DJR |
| Device type | Enzyme Immunoassay, Methadone |
| Device class | Class 2 |
| Regulation | 21 CFR 862.3620 |
| Establishment | Manufacturer, Exporter |
| 510(k) | K182779 |
| Record published | 2019-01-21 |
Specifications
| MRI safety | Labeling does not contain MRI Safety Information |
|---|---|
| Single use | Yes |
| Prescription | Prescription only |
| Supplied as a kit | Yes |
| Label carries | lot or batch number, expiry date |
| Storage | Storage environment temperature 2 to 8 °C |
Catalogue Numbers
| Catalogue number | Size | Status |
|---|---|---|
| 5051-0001-00 | In distribution |
Same Product Code
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| Healgen | Healgen Scientific Limited Liability Company | 56 |
| Identify Diagnostics Drug Test Cups | Medical Distribution Group Inc | 23 |
| DOA 5 Panel Test | Rapid Diagnostics, Inc. | 20 |
| Advin Multi-Drug Screen Test | Advin Biotech, Inc. | 14 |
| ProScreen | Instant Tech Subsidiary Acquisition | 13 |
| DrugCheck | Express Diagnostics Int’l., Inc. | 12 |
| UCP Compact Drug Test Cups | UCP Biosciences, Inc. | 12 |
| MD DugScreen | Medical Disposables Corp | 12 |
| CLIAwaived | Cliawaived,inc. | 11 |
| QuickTox Drug Screen Dipcard | Branan Medical Corporation | 10 |
| U-Screen | Instant Tech Subsidiary Acquisition | 7 |
| First Sign® | Hemosure Inc. | 7 |
Showing 12 of 170. All products under Enzyme Immunoassay, Methadone
510(K) Clearances
| Clearance | Decision date |
|---|---|
| K182779 | 2018-11-21 |
Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.