Instant Test Cup

THC50, COC300, OPI300, AMP1000, MET1000, PCP25, MDMA500, BAR300, BZO300, MTD300, TCA1000, OXY100 Drugs of Abuse Test Cup (CLIA WAIVED)

Registry build 21.09.26
17manufacturers in China registered for this device type
2catalogue numbers in this listing
2510(k) clearances naming this product code
1recall

Who Else Makes It

Concentrated in Zhejiang (9), Guangdong (4), Beijing (2). 5 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code DJG
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
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
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

Showing 12 of 17. All 17 manufacturers in China registered for Enzyme Immunoassay, Opiates

Record

Regulatory record for Instant Test Cup
Listed by Ameditech, Inc., United States
FDA product code DJG
Device type Enzyme Immunoassay, Opiates
Device class Class 2
Regulation 21 CFR 862.3650
Establishment Complaint-file establishment, Manufacturer
510(k) K082898
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
Over the counter Yes
Supplied as a kit Yes
Label carries lot or batch number, expiry date
Storage Storage environment temperature 2 to 30 °C; Storage environment temperature 36 to 86 °F
Distribution end date 2018-09-20

Catalogue Numbers

Catalogue numbers for Instant Test Cup
Catalogue number Size Status
10-100 Withdrawn
10-300 Withdrawn

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Advin Multi-Drug Screen Test Advin Biotech, Inc. 75
MD DugScreen Medical Disposables Corp 37
Immunalysis Immunalysis Corporation 37
DrugCheck Express Diagnostics Int’l., Inc. 29
DOA 6 Panel Test Rapid Diagnostics, Inc. 28
First Sign® Hemosure Inc. 20
Enzyme Immunoassay, Opiates W.h.p.m., Inc. 20
DrugCheck Express Diagnostic Int’l, Inc. 19
MD DrugScreen Medical Disposables Corp 18
DOA-7 Panel Test Rapid Diagnostics, Inc. 18
DOA 5 Panel Test Rapid Diagnostics, Inc. 16
Rapid Response Btnx Inc. 14

Showing 12 of 316. All products under Enzyme Immunoassay, Opiates

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K063015 2006-12-20
K012483 2001-11-30

Recalls Naming This Product

1 recall names this product by its own identifier, the 510(k) it is cleared under.

Recalls naming the identifiers of Instant Test Cup
Recalled by Identified by Initiated FDA class Root cause Reason Quantity Closed
Ameditech, Inc. 510(k) number 2017-09-30 Class III Nonconforming Material/Component Product was released to market without the adulteration strip included in the product. 40 kit boxes (1000 units) 2019-08-06

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.

Recalls referencing this product code
Initiated FDA class Root cause Reason Quantity Closed
2019-02-15 Class III Labeling mix-ups Mixed Products containing QuickTox 5 Panel Drugs Screen Dipcard (P/N QT11, LOT #188787) and Alere iScreen Drugs of Abuse Dip Test (P/N X11-IS10-22015-DX LOT #188744) 3400 units (136 kits) 2021-04-28

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