Barbiturates Intercept 2 Plate Kit
Catalogue number 1108IT, listed by Orasure Technologies, Inc., United States, under Enzyme Immunoassay, Barbiturate. 12 manufacturers in China are registered for this product code.
Who Else Makes It
Concentrated in Zhejiang (6), Guangdong (3), 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 |
| Guangzhou Wondfo Biotech Co., Ltd. | Guangzhou | Guangdong | Contract manufacturer | 44 |
| 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 | Orasure Technologies, Inc., United States |
|---|---|
| FDA product code | DIS |
| Device type | Enzyme Immunoassay, Barbiturate |
| Device class | Class 2 |
| Regulation | 21 CFR 862.3150 |
| Establishment | Contract manufacturer, Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer |
| Record published | 2016-09-12 |
| Record revised | 2026-05-05 (version 4) |
Specifications
| MRI safety | Labeling does not contain MRI Safety Information |
|---|---|
| Prescription | Prescription only |
| Supplied as a kit | Yes |
| Label carries | lot or batch number, expiry date |
| Storage | Storage environment temperature 2 to 8 °C |
| Distribution end date | 2025-04-04 |
| UDI direct marking | Exempt |
Catalogue Numbers
| Catalogue number | Size | Status |
|---|---|---|
| 1108IT | Withdrawn |
Same Product Code
| Product | Sold by | Catalogue numbers |
|---|---|---|
| MD DugScreen | Medical Disposables Corp | 9 |
| DrugCheck | Express Diagnostics Int’l., Inc. | 7 |
| Healgen | Healgen Scientific Limited Liability Company | 6 |
| ProScreen | Instant Tech Subsidiary Acquisition | 5 |
| EZ-Screen® CUP | Medtox Diagnostics, Inc. | 5 |
| Immunalysis | Immunalysis Corporation | 4 |
| DrugCheck | Express Diagnostic Int’l, Inc. | 4 |
| MD DrugScreen | Medical Disposables Corp | 4 |
| QuickTox Drug Screen Dipcard | Ameditech, Inc. | 4 |
| TOX/See | Bio-Rad Laboratories Inc. | 3 |
| DRI Barbiturate Assay | Microgenics Corporation | 3 |
| QuickTox Drug Screen Dipcard | Branan Medical Corporation | 3 |
Showing 12 of 102. All products under Enzyme Immunoassay, Barbiturate
510(K) Clearances
| Clearance | Decision date |
|---|---|
| K001976 | 2000-12-06 |
| K982745 | 1998-11-18 |
Recalls
1 of these is Class III. Class III is unlikely to cause harm at all → typically a labelling or documentation fault. Volume alone is not a quality signal: a manufacturer that ships more recalls more.
| Initiated | FDA class | Root cause | Reason | Quantity | Closed |
|---|---|---|---|---|---|
| 2016-11-10 | Class III | Mixed-up of materials/components | Shipping error. Cocaine metabolite Microplate distributed instead of Barbiturate Microplate due to incorrect selection of Microplate during manufacturing. | 4 kits | 2017-04-17 |
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.