Xreader System

The xReader System consists of a small, portable high resolution flatbed scanner, customized Software, and lateral flow tests that are intended for use in the system. The scanner has a…

Registry build 21.09.26

The xReader System consists of a small, portable high resolution flatbed scanner, customized Software, and lateral flow tests that are intended for use in the system. The scanner has a custom Scanner Lid with an opening for the test device, and a Scanner Stand, which places the scanner bed at the appropriate angle for running and reading the test devices. The xReader System is intended for use with the xCup, which is a rapid, single use, disposable immunochromatographic test for the qualitative detection of drugs of abuse in human urine. The xReader System detects drug classes at the following cutoff concentrations: Amphetamines at 500 ng/mL; Barbiturates at 300 ng/mL; Benzodiazepines at 300 ng/mL; Cocaine at 150 ng/mL; Methamphetamines at 500 ng/mL; Methadone at 300 ng/mL; Morphine at 300 ng/mL and 2000 ng/mL; Oxycodone at 100 ng/mL; Phencyclidine at 25 ng/mL; and Marijuana at 50 ng/mL. Configurations of the xCup may consist of any combination of the listed drug analytes. The xCup test devices are run in the xReader System according to their specific instructions for use. At the conclusion of the test an image is captured and the Software determines whether the colored test lines for each analyte are above or below the threshold associated with a Send to Lab or a Discard result. The Software also confirms the validity of the results by verifying the presence of control lines and analyzing the specimen validity. The xReader System is for in vitro diagnostic use and is intended for use in laboratories, point-of-care sites and workplaces by minimally trained users. The test is not intended for over-the-counter use. The xCup test devices cannot be read visually.

18manufacturers in China registered for this device type
1catalogue number

Who Else Makes It

Concentrated in Zhejiang (9), Guangdong (4), Beijing (2). 6 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code LDJ
Manufacturer City Province Registered as Device types
Zhejiang Orient Gene Biotech Huzhou Zhejiang Contract manufacturer 86
Assure Tech. (Hangzhou) Co., Ltd. Hangzhou Zhejiang Contract manufacturer 48
Hangzhou Biotest Biotech Co., Ltd. Hangzhou Zhejiang Contract manufacturer 41
Abon Biopharm (Hangzhou) Co., Ltd. Hangzhou Zhejiang Contract manufacturer 17
Core Technology Co., Ltd. Changping District Beijing Contract manufacturer 14
Prometheus Bio Inc. Hangzhou Zhejiang Contract manufacturer 12
Hangzhou AllTest Biotech 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

Showing 12 of 18. All 18 manufacturers in China registered for Enzyme Immunoassay, Cannabinoids

Record

Regulatory record for xReader System
Listed by Escreen, Inc., United States
FDA product code LDJ
Device type Enzyme Immunoassay, Cannabinoids
Device class Class 2
Regulation 21 CFR 862.3870
510(k) K130082
Record published 2016-09-16
Record revised 2022-03-08 (version 6)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Prescription Prescription only
Supplied as a kit Yes
Label carries serial number
Storage Storage environment temperature 15 to 35 °C; Handling environment temperature 15 to 35 °C

Catalogue Numbers

Catalogue numbers for xReader System
Catalogue number Size Status
BS-0610S In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
DrugCheck Express Diagnostics Int’l., Inc. 378
Advin Multi-Drug Screen Test Advin Biotech, Inc. 234
DrugCheck Express Diagnostic Int’l, Inc. 167
T-Cup Wondfo USA Co., Ltd. 63
Wondfo Drug Test Dip Card Wondfo USA Co., Ltd. 56
Enzyme Immunoassay, Cannabinoids Alere San Diego, Inc. 48
Premier Bio-Cup & Bio-Dip Premier Biotech, LLC 46
Enzyme Immunoassay, Cannabinoids W.h.p.m., Inc. 35
MD DugScreen Medical Disposables Corp 24
AllSource Screening Solutions – Drug Detector Allsource Screening Solutions 18
Preview Wondfo USA Co., Ltd. 18
Identify Diagnostics Drug Test Cups Medical Distribution Group Inc 17

Showing 12 of 288. All products under Enzyme Immunoassay, Cannabinoids

PMA Approvals

A premarket approval is the full Class III route, granted on clinical evidence rather than on equivalence to an existing device. It is the highest regulatory bar a device of this type can clear.

FDA premarket approvals naming this product code
PMA number Decision Trade name Approved to
P950040 1997-01-21 DR. BROWN’S HOME DRUG TESTING KIT Personal Health & Hygiene, Inc.

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.

Where China Actually Supplies

Every device page names the company that lists it and the factories registered to make the same thing. These are the sections with the most of them.

5,100manufacturers registered in China
2,581device types they are registered for
340,248device records, each naming its maker
31provinces with a registered manufacturer