ToxCup Drug Screen Cup

AMP1000/COC300/BAR300/BZO300/MTD300/OXY100/OPI300 Adulteration Screen for CR-NI-PH-BL-SG

Registry build 21.09.26
11manufacturers in China registered for this device type
1catalogue number

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.

Chinese manufacturers registered for FDA product code DJR
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

Regulatory record for ToxCup Drug Screen Cup
Listed by Ameditech, Inc., United States
FDA product code DJR
Device type Enzyme Immunoassay, Methadone
Device class Class 2
Regulation 21 CFR 862.3620
Establishment Complaint-file establishment, Manufacturer
510(k) K032057
Record published 2017-03-31
Record revised 2023-11-14 (version 7)

Specifications

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 15 to 30 °C; Handling environment temperature 15 to 30 °C
Distribution end date 2020-10-09

Catalogue Numbers

Catalogue numbers for ToxCup Drug Screen Cup
Catalogue number Size Status
HT32A Withdrawn

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
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

Recalls Naming This Product

2 recalls name this product by its own identifiers, the 510(k) it is cleared under.

Recalls naming the identifiers of ToxCup Drug Screen Cup
Recalled by Identified by Initiated FDA class Root cause Reason Quantity Closed
Ameditech, Inc. 510(k) number 2020-08-18 Class II Process control Various immunoassay enzymes failed product performance, thereby the products do not consistently detect all calibrator and secondary compounds at the levels stated in the labeling. 189,175 units 2024-09-30
Branan Medical Corporation 510(k) number 2014-03-26 Class II Labeling Change Control May be labeled with incorrect result interpretation graphics on the ToxCup lid label. 9,800 units 2014-07-23

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