EZ-Screen® CUP

A qualitative one-step immunochromatographic test panel for the detection of THC (Cannabinoids), Opiates, Methamphetamine, Cocaine, Phencyclidine, Amphetamine, Benzodiazepines, Methadone,…

Registry build 21.09.26

A qualitative one-step immunochromatographic test panel for the detection of THC (Cannabinoids), Opiates, Methamphetamine, Cocaine, Phencyclidine, Amphetamine, Benzodiazepines, Methadone, Barbiturates, Oxycodone, and Buprenorphine drugs and/or their metabolites in human urine.

12manufacturers in China registered for this device type
5catalogue numbers in this listing
4510(k) clearances naming 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.

Chinese manufacturers registered for FDA product code DIS
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

Regulatory record for EZ-Screen® CUP
Listed by Medtox Diagnostics, Inc., United States
FDA product code DIS
Device type Enzyme Immunoassay, Barbiturate
Device class Class 2
Regulation 21 CFR 862.3150
Establishment Specification developer, Manufacturer, Exporter
510(k) K002331
Record published 2016-09-16
Record revised 2022-06-10 (version 6)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Single use Yes
Prescription Prescription only
Label carries lot or batch number, expiry date
Storage Storage environment temperature 2 to 25 °C
Packaging Kit box of 25
Distribution end date 2016-09-16

Catalogue Numbers

Catalogue numbers for EZ-Screen® CUP
Catalogue number Size Status
605212 In distribution
605102 In distribution
605204 In distribution
605203 In distribution
605106 Withdrawn

Same Product Code

Other products under the same FDA 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
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
CRL Stat Cup Clinical Reference Laboratory, Inc. 3

Showing 12 of 102. All products under Enzyme Immunoassay, Barbiturate

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K033334 2003-11-10
K010959 2001-04-13
K010561 2001-04-05
K002331 2001-01-17

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.

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