Enzyme Immunoassay, Cannabinoids

DOA 10 in 1 Test Dipcard W/AD, 25Pcs/Box Clia Waived AMP/BARB/BZO/COC/mAMP/MDMA/MOR/MTD/OXY/THC/PH-SG-OX

Registry build 21.09.26
18manufacturers in China registered for this device type
35catalogue numbers in this listing

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 Enzyme Immunoassay, Cannabinoids
Listed by W.h.p.m., Inc., United States
FDA product code LDJ
Device type Enzyme Immunoassay, Cannabinoids
Device class Class 2
Regulation 21 CFR 862.3870
Establishment Contract manufacturer, Manufacturer
Record published 2018-01-10
Record revised 2022-11-28 (version 5)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Single use Yes
Prescription Prescription only
Over the counter Yes
Supplied as a kit Yes
Label carries lot or batch number, expiry date

Catalogue Numbers

Catalogue numbers for Enzyme Immunoassay, Cannabinoids
Catalogue number Size Per pack Status
W13124 25 In distribution
W2874 25 In distribution
W1834 25 In distribution
W954 25 In distribution
W334 25 In distribution
W3104 25 In distribution
W154RD 25 In distribution
W14104 W/AD 25 In distribution
WCUP1434 25 In distribution
WDCA244 25 In distribution
W6104 25 In distribution
D4-D04-100 100 In distribution
W744 25 In distribution
W1064 25 In distribution
W1384 25 In distribution
W2124 25 In distribution
W5064 25 In distribution
WTH-25 25 In distribution
W4054 25 In distribution
W20104 25 In distribution
W1574 25 In distribution
W244 25 In distribution
W14104 25 In distribution
W2334 25 In distribution
WCUP254 W/AD 25 In distribution
W674 25 In distribution
W134 25 In distribution
W8104 25 In distribution
W1924 25 In distribution
W424 25 In distribution
W654 25 In distribution
W154 25 In distribution
W234 25 In distribution
W464 25 In distribution
W22104 25 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
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
ImmuTest Drugs of abuse Cup Ameditech, 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